geneid | 27247 |
---|---|
ensemblid | ENSG00000169599.13 |
hgncid | 16287 |
symbol | NFU1 |
name | NFU1 iron-sulfur cluster scaffold |
refseq_nuc | NM_001002755.4 |
refseq_prot | NP_001002755.1 |
ensembl_nuc | ENST00000410022.7 |
ensembl_prot | ENSP00000387219.3 |
mane_status | MANE Select |
chr | chr2 |
start | 69396126 |
end | 69437435 |
strand | - |
ver | v1.2 |
region | chr2:69396126-69437435 |
region5000 | chr2:69391126-69442435 |
regionname0 | NFU1_chr2_69396126_69437435 |
regionname5000 | NFU1_chr2_69391126_69442435 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 254 | 259 | 63 | 38 | 131 | 5 | 21 | 98 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0002 | 0/1 | 254 | 100 | 25 | 19 | 41 | 4 | 10 | 30 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0003 | 0/0 | 254 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0004 | 0/0 | 254 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 765 | 250 | 63 | 29 | 131 | 5 | 21 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
c0002 | 0/1 | 765 | 100 | 25 | 19 | 41 | 4 | 10 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
c0003 | 0/0 | 765 | 9 | 0 | 9 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
c0004 | 0/0 | 765 | 5 | 4 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
c0005 | 0/0 | 765 | 4 | 0 | 2 | 0 | 1 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 765 | 250 | 63 | 29 | 131 | 5 | 21 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0001c0003 | 0/0 | 765 | 9 | 0 | 9 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0002c0002 | 0/1 | 765 | 100 | 25 | 19 | 41 | 4 | 10 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0003c0004 | 0/0 | 765 | 5 | 4 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0004c0005 | 0/0 | 765 | 4 | 0 | 2 | 0 | 1 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 898 | 249 | 62 | 29 | 131 | 5 | 21 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0001c0001t0002 | 0/0 | 898 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0001c0003t0001 | 0/0 | 898 | 9 | 0 | 9 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0002c0002t0001 | 0/1 | 898 | 100 | 25 | 19 | 41 | 4 | 10 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0003c0004t0001 | 0/0 | 898 | 5 | 4 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
a0004c0005t0001 | 0/0 | 898 | 4 | 0 | 2 | 0 | 1 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | copy fasta | chr2 | 69391126 | 69442435 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0001 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0297 | EUR | GBR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0212 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0211 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01106 | hp2 | a0004 | c0005 | t0001 | g0096 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0327 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0326 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0344 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01243 | hp1 | a0003 | c0004 | t0001 | g0145 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0259 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0345 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01516 | hp2 | a0004 | c0005 | t0001 | g0067 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0335 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0321 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0314 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0235 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01981 | hp1 | a0004 | c0005 | t0001 | g0091 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0292 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0173 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0338 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | CDX | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0288 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0265 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0268 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0334 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0325 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0358 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0357 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0324 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0141 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0323 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0279 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0336 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0309 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03927 | hp2 | a0004 | c0005 | t0001 | g0092 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0339 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0143 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0333 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | ASW | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | ASW | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0341 | SAS | GIH | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | GIH | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG06807 | hp2 | a0003 | c0004 | t0001 | g0144 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA21309 | hp1 | a0003 | c0004 | t0001 | g0142 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0001 | REF | REF | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69423598
|
G | A | 1 | a0004 | 4 | HG01106.hp2 HG01516.hp2 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.286C>T | p.Arg96Cys | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/8 | 299/898 | 286/765 | 96/254 | chr2 | 69423598 | ||
chr2:69431917
|
C | A | 1 | a0003 | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
missense_variant | MODERATE | c.151G>T | p.Ala51Ser | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/8 | 164/898 | 151/765 | 51/254 | chr2 | 69431917 | ||
chr2:69431994
|
A | T | 1 | a0002 | 100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
missense_variant | MODERATE | c.74T>A | p.Met25Lys | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/8 | 87/898 | 74/765 | 25/254 | chr2 | 69431994 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69415258
|
A | G | 1 | a0001c0003 | 9 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(6): Show |
synonymous_variant | LOW | c.411T>C | p.Ile137Ile | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/8 | 424/898 | 411/765 | 137/254 | chr2 | 69415258 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69437428
|
T | C | 1 | a0001c0001t0002 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/8 | 6 | chr2 | 69437428 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69396515
|
G | C | 1 | a0002c0002t0001g0342 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.721-225C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396515 | ||||||
chr2:69396543
|
C | T | 1 | a0003c0004t0001g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.721-253G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396543 | ||||||
chr2:69396546
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-256C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396546 | ||||||
chr2:69396624
|
G | A | 1 | a0002c0002t0001g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.721-334C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396624 | ||||||
chr2:69396734
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-444C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396734 | ||||||
chr2:69396800
|
C | T | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.721-510G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396800 | ||||||
chr2:69396801
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-511C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396801 | ||||||
chr2:69396843
|
C | T | 1 | a0002c0002t0001g0307 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.721-553G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396843 | ||||||
chr2:69396844
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.721-554T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396844 | ||||||
chr2:69396897
|
C | T | 1 | a0002c0002t0001g0330 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.721-607G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396897 | ||||||
chr2:69396973
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.721-683T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396973 | ||||||
chr2:69397045
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.721-755T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397045 | ||||||
chr2:69397073
|
C | CA | 12 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 13 | HG02080.hp2 HG02257.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-784dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397073 | ||||||
chr2:69397203
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.721-913T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397203 | ||||||
chr2:69397242
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(240): Show | 248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.721-952C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397242 | ||||||
chr2:69397248
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.721-958G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397248 | ||||||
chr2:69397264
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.721-974T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397264 | ||||||
chr2:69397446
|
C | T | 133 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(130): Show | 136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.721-1156G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397446 | ||||||
chr2:69397581
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.721-1291A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397581 | ||||||
chr2:69397616
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0046 | 2 | HG00609.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.721-1326A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397616 | ||||||
chr2:69397616
|
T | TA | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 51 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.721-1327_721-1326i others(3): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397616 | ||||||
chr2:69397617
|
T | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 53 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.721-1327A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397617 | ||||||
chr2:69397617
|
T | TA | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(155): Show | 162 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.721-1328_721-1327i others(3): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397617 | ||||||
chr2:69397618
|
T | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(215): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.721-1328A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397618 | ||||||
chr2:69397618
|
T | TA | 23 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(20): Show | 23 | HG00558.hp1 HG00642.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.721-1329dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397618 | ||||||
chr2:69397618
|
T | TAA | 6 | a0001c0001t0001g0050a0003c0004t0001g0141a0003c0004t0001g0142others(3): Show | 6 | HG01243.hp1 HG01433.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-1330_721-1329d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397618 | ||||||
chr2:69397702
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.721-1412G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397702 | ||||||
chr2:69397721
|
C | T | 1 | a0002c0002t0001g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.721-1431G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397721 | ||||||
chr2:69397869
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.721-1579T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397869 | ||||||
chr2:69397914
|
CA | C | 49 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(46): Show | 49 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.721-1625delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397914 | ||||||
chr2:69397914
|
CAA | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(147): Show | 154 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.721-1626_721-1625d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397914 | ||||||
chr2:69397914
|
CAAA | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 44 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.721-1627_721-1625d others(5): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397914 | ||||||
chr2:69397980
|
C | A | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-1690G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397980 | ||||||
chr2:69398025
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.721-1735G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398025 | ||||||
chr2:69398069
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.721-1779G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398069 | ||||||
chr2:69398085
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.721-1795T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398085 | ||||||
chr2:69398278
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721-1988T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398278 | ||||||
chr2:69398365
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.720+1999T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398365 | ||||||
chr2:69398403
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1961G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398403 | ||||||
chr2:69398506
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.720+1858A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398506 | ||||||
chr2:69398546
|
CT | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.720+1817delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398546 | ||||||
chr2:69398623
|
T | C | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.720+1741A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398623 | ||||||
chr2:69398660
|
T | A | 1 | a0002c0002t0001g0256 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.720+1704A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398660 | ||||||
chr2:69398860
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0041 | 3 | NA18954.hp1 NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.720+1504A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398860 | ||||||
chr2:69398896
|
A | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.720+1468T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398896 | ||||||
chr2:69398977
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0208a0001c0001t0001g0233 | 3 | NA18954.hp2 NA18992.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.720+1387G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69398977 | ||||||
chr2:69399123
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.720+1241C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399123 | ||||||
chr2:69399200
|
A | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0182a0001c0001t0001g0237others(2): Show | 5 | HG00639.hp2 HG00741.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+1164T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399200 | ||||||
chr2:69399210
|
C | CA | 22 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0050others(19): Show | 22 | HG01433.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.720+1153dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399210 | ||||||
chr2:69399265
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | NA19004.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.720+1099A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399265 | ||||||
chr2:69399322
|
T | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.720+1042A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399322 | ||||||
chr2:69399369
|
G | A | 1 | a0002c0002t0001g0341 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.720+995C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399369 | ||||||
chr2:69399555
|
G | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.720+809C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399555 | ||||||
chr2:69399598
|
G | T | 2 | a0003c0004t0001g0142a0003c0004t0001g0145 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.720+766C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399598 | ||||||
chr2:69399615
|
C | CA | 14 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0033others(11): Show | 14 | HG02080.hp1 HG02145.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+748dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399615 | ||||||
chr2:69399645
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+719A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399645 | ||||||
chr2:69399723
|
T | G | 3 | a0002c0002t0001g0264a0002c0002t0001g0339a0002c0002t0001g0341 | 3 | HG04115.hp1 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.720+641A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399723 | ||||||
chr2:69399876
|
AT | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(229): Show | 237 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.720+487delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399876 | ||||||
chr2:69399933
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 51 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.720+431G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399933 | ||||||
chr2:69399941
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.720+423G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399941 | ||||||
chr2:69399996
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 51 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.720+368G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399996 | ||||||
chr2:69400067
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.720+297A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69400067 | ||||||
chr2:69400705
|
A | AT | 135 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(132): Show | 138 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.546-168dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400705 | ||||||
chr2:69400744
|
C | T | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.546-206G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400744 | ||||||
chr2:69400764
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-226C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400764 | ||||||
chr2:69400768
|
A | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-230T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400768 | ||||||
chr2:69400770
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.546-232G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400770 | ||||||
chr2:69400787
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.546-249C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400787 | ||||||
chr2:69400815
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.546-277A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400815 | ||||||
chr2:69400906
|
C | T | 3 | a0002c0002t0001g0270a0002c0002t0001g0284a0002c0002t0001g0302 | 3 | HG00408.hp2 HG02015.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.546-368G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400906 | ||||||
chr2:69400957
|
A | T | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.546-419T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400957 | ||||||
chr2:69400966
|
A | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.546-428T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400966 | ||||||
chr2:69401359
|
T | G | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.546-821A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69401359 | ||||||
chr2:69401468
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(134): Show | 140 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.546-930A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69401468 | ||||||
chr2:69401898
|
CT | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(133): Show | 139 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.546-1361delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69401898 | ||||||
chr2:69402013
|
A | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(245): Show | 253 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.546-1475T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402013 | ||||||
chr2:69402421
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(244): Show | 252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.546-1883T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402421 | ||||||
chr2:69402569
|
C | G | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.546-2031G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402569 | ||||||
chr2:69402641
|
G | C | 2 | a0002c0002t0001g0276a0002c0002t0001g0337 | 2 | NA18953.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.546-2103C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402641 | ||||||
chr2:69402674
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.546-2136G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402674 | ||||||
chr2:69402675
|
G | A | 41 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(38): Show | 41 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.546-2137C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402675 | ||||||
chr2:69402873
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.546-2335C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402873 | ||||||
chr2:69402879
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546-2341C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402879 | ||||||
chr2:69402905
|
G | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0152others(33): Show | 38 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.546-2367C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402905 | ||||||
chr2:69402910
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.546-2372C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402910 | ||||||
chr2:69402966
|
TTTCTC | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.546-2433_546-2429d others(7): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402966 | ||||||
chr2:69403379
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.545+2643C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403379 | ||||||
chr2:69403427
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(245): Show | 253 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.545+2595T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403427 | ||||||
chr2:69403503
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+2519C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403503 | ||||||
chr2:69403673
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.545+2349C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403673 | ||||||
chr2:69403828
|
T | C | 1 | a0001c0001t0001g0360 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.545+2194A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403828 | ||||||
chr2:69403835
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.545+2187G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403835 | ||||||
chr2:69403843
|
C | CT | 47 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 48 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.545+2178dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403843 | ||||||
chr2:69403843
|
CT | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 8 | HG00323.hp2 HG01256.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.545+2178delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403843 | ||||||
chr2:69403924
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.545+2098G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403924 | ||||||
chr2:69403964
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.545+2058C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403964 | ||||||
chr2:69403988
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+2034C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403988 | ||||||
chr2:69404006
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.545+2016A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404006 | ||||||
chr2:69404118
|
G | A | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+1904C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404118 | ||||||
chr2:69404214
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.545+1808C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404214 | ||||||
chr2:69404309
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.545+1713G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404309 | ||||||
chr2:69404351
|
G | T | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.545+1671C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404351 | ||||||
chr2:69404440
|
T | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.545+1582A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404440 | ||||||
chr2:69404447
|
G | A | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.545+1575C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404447 | ||||||
chr2:69404503
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.545+1519A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404503 | ||||||
chr2:69404511
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.545+1511G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404511 | ||||||
chr2:69404564
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.545+1458G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404564 | ||||||
chr2:69404565
|
G | A | 6 | a0001c0001t0001g0003a0003c0004t0001g0141a0003c0004t0001g0142others(3): Show | 7 | HG01243.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1457C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404565 | ||||||
chr2:69404568
|
T | C | 1 | a0002c0002t0001g0302 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.545+1454A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404568 | ||||||
chr2:69404615
|
A | AT | 11 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0207others(8): Show | 11 | HG01175.hp1 HG01978.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.545+1406dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATATTTTT others(3): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0095a0001c0001t0001g0140 | 3 | HG02132.hp1 HG03195.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.545+1406_545+1407i others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATATTTTT others(4): Show |
22 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(19): Show | 22 | HG00558.hp1 HG01074.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.545+1406_545+1407i others(13): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATATTTTT others(5): Show |
10 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0075others(7): Show | 10 | HG01106.hp2 HG01891.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.545+1406_545+1407i others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0348a0003c0004t0001g0142a0003c0004t0001g0143others(1): Show | 4 | HG01243.hp1 HG01928.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+1397_545+1406d others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0349a0003c0004t0001g0141 | 3 | HG00642.hp1 HG01109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.545+1396_545+1406d others(13): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0100a0003c0004t0001g0144 | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+1395_545+1406d others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0101 | 2 | HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.545+1394_545+1406d others(15): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0060 | 2 | HG03471.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.545+1393_545+1406d others(16): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(8): Show |
22 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(19): Show | 22 | HG00544.hp2 HG00621.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.545+1392_545+1406d others(17): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(9): Show |
41 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0028others(38): Show | 44 | HG00597.hp1 HG00738.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.545+1391_545+1406d others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(10): Show |
25 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0030others(22): Show | 25 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.545+1390_545+1406d others(19): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(11): Show |
10 | a0001c0001t0001g0050a0001c0001t0001g0066a0001c0001t0001g0124others(7): Show | 10 | HG01109.hp1 HG01433.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.545+1389_545+1406d others(20): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(12): Show |
6 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+1388_545+1406d others(21): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(13): Show |
5 | a0001c0001t0001g0038a0001c0001t0001g0125a0002c0002t0001g0287others(2): Show | 5 | HG01884.hp2 HG02738.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1387_545+1406d others(22): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(14): Show |
7 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0019others(4): Show | 7 | HG01167.hp1 HG02027.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1386_545+1406d others(23): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(15): Show |
7 | a0001c0001t0001g0033a0001c0001t0001g0041a0002c0002t0001g0274others(4): Show | 7 | HG00408.hp2 HG02015.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+1385_545+1406d others(24): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(16): Show |
5 | a0002c0002t0001g0269a0002c0002t0001g0270a0002c0002t0001g0276others(2): Show | 5 | HG03225.hp1 NA18953.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1384_545+1406d others(25): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(17): Show |
6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG02040.hp1 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+1406_545+1407i others(26): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(18): Show |
1 | a0002c0002t0001g0334 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.545+1406_545+1407i others(27): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(19): Show |
2 | a0002c0002t0001g0357a0002c0002t0001g0358 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.545+1406_545+1407i others(28): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
A | ATTTTTTT others(31): Show |
1 | a0001c0001t0001g0123 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.545+1406_545+1407i others(40): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
AT | A | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 15 | HG00735.hp1 HG01069.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.545+1406delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404615
|
ATTTTT | A | 25 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(22): Show | 25 | HG01884.hp1 HG02074.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.545+1402_545+1406d others(7): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404615 | ||||||
chr2:69404776
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0002g0361 | 2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.545+1246G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404776 | ||||||
chr2:69404777
|
G | A | 97 | a0001c0001t0001g0060a0002c0002t0001g0001a0002c0002t0001g0006others(94): Show | 100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.545+1245C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404777 | ||||||
chr2:69404797
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.545+1225G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404797 | ||||||
chr2:69404872
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.545+1150G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404872 | ||||||
chr2:69405113
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.545+909C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405113 | ||||||
chr2:69405346
|
C | T | 1 | a0002c0002t0001g0307 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.545+676G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405346 | ||||||
chr2:69405488
|
T | C | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.545+534A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405488 | ||||||
chr2:69405561
|
G | C | 1 | a0002c0002t0001g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.545+461C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405561 | ||||||
chr2:69405692
|
T | C | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+330A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405692 | ||||||
chr2:69405724
|
CT | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+297delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405724 | ||||||
chr2:69405804
|
T | C | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+218A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405804 | ||||||
chr2:69405868
|
T | A | 1 | a0002c0002t0001g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.545+154A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69405868 | ||||||
chr2:69406250
|
A | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.485-168T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406250 | ||||||
chr2:69406287
|
C | G | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.485-205G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406287 | ||||||
chr2:69406356
|
G | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0084others(3): Show | 6 | HG02976.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-274C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406356 | ||||||
chr2:69406378
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-296T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406378 | ||||||
chr2:69406431
|
G | GA | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.485-350dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406431 | ||||||
chr2:69406528
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485-446T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406528 | ||||||
chr2:69406619
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.485-537C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406619 | ||||||
chr2:69406629
|
G | A | 2 | a0002c0002t0001g0309a0002c0002t0001g0317 | 2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.485-547C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406629 | ||||||
chr2:69406666
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.485-584C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406666 | ||||||
chr2:69406864
|
G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0039 | 3 | NA18956.hp2 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.485-782C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406864 | ||||||
chr2:69406933
|
G | T | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-851C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406933 | ||||||
chr2:69406941
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.485-859G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406941 | ||||||
chr2:69406962
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02559.hp2 HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.485-880G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406962 | ||||||
chr2:69407030
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.485-948T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407030 | ||||||
chr2:69407407
|
T | C | 1 | a0001c0001t0001g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-1325A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407407 | ||||||
chr2:69407492
|
T | C | 1 | a0002c0002t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.485-1410A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407492 | ||||||
chr2:69407503
|
C | G | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.485-1421G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407503 | ||||||
chr2:69407603
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.485-1521A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407603 | ||||||
chr2:69407669
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0088 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.485-1587A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407669 | ||||||
chr2:69407674
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(7): Show | 12 | HG00597.hp2 HG00609.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.485-1593dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407674 | ||||||
chr2:69407674
|
CA | C | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(204): Show | 210 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.485-1593delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407674 | ||||||
chr2:69407688
|
AAAAGAAA others(8): Show |
A | 21 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.485-1621_485-1607d others(17): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407688 | ||||||
chr2:69407706
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.485-1624T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407706 | ||||||
chr2:69407787
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.485-1705G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407787 | ||||||
chr2:69407788
|
G | A | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485-1706C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407788 | ||||||
chr2:69407790
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.485-1708C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407790 | ||||||
chr2:69407962
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-1880C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407962 | ||||||
chr2:69407968
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.485-1886C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69407968 | ||||||
chr2:69408012
|
CA | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 235 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.485-1931delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408012 | ||||||
chr2:69408012
|
CAA | C | 10 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-1932_485-1931d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408012 | ||||||
chr2:69408333
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485-2251A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408333 | ||||||
chr2:69408498
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485-2416A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408498 | ||||||
chr2:69408547
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485-2465G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408547 | ||||||
chr2:69408652
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485-2570C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408652 | ||||||
chr2:69408671
|
G | A | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.485-2589C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408671 | ||||||
chr2:69408701
|
C | CAG | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.485-2621_485-2620d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408701 | ||||||
chr2:69408734
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0239 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.485-2652A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
T | TTA | 8 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189others(5): Show | 8 | HG00140.hp1 HG01255.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.485-2654_485-2653d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0178 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.485-2664_485-2653d others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0180 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.485-2668_485-2653d others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTA | T | 59 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.485-2654_485-2653d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTATA | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0169others(13): Show | 17 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.485-2656_485-2653d others(6): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTATATAT others(5): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0001g0129 | 2 | NA18988.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.485-2664_485-2653d others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTATATAT others(7): Show |
T | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.485-2666_485-2653d others(16): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTATATAT others(9): Show |
T | 139 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(136): Show | 142 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.485-2668_485-2653d others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408734
|
TTATATAT others(11): Show |
T | 14 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101others(11): Show | 15 | HG01109.hp2 HG01884.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.485-2670_485-2653d others(20): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408734 | ||||||
chr2:69408769
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0166a0001c0001t0001g0229others(2): Show | 5 | HG01361.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2687A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408769 | ||||||
chr2:69408861
|
C | CT | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0035others(22): Show | 25 | HG00621.hp1 HG00735.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.485-2780dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408861 | ||||||
chr2:69408861
|
C | CTT | 33 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.485-2781_485-2780d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408861 | ||||||
chr2:69408861
|
CT | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0044others(99): Show | 106 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.485-2780delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408861 | ||||||
chr2:69408885
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485-2803C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408885 | ||||||
chr2:69408886
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485-2804T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408886 | ||||||
chr2:69408887
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485-2805G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408887 | ||||||
chr2:69408887
|
CAG | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 42 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.485-2807_485-2806d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408887 | ||||||
chr2:69408889
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485-2807C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408889 | ||||||
chr2:69409019
|
T | C | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-2937A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409019 | ||||||
chr2:69409061
|
T | G | 1 | a0002c0002t0001g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-2979A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409061 | ||||||
chr2:69409102
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.485-3020T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409102 | ||||||
chr2:69409132
|
G | A | 2 | a0001c0001t0001g0139a0002c0002t0001g0286 | 2 | HG00735.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.485-3050C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409132 | ||||||
chr2:69409516
|
G | A | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.485-3434C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409516 | ||||||
chr2:69409567
|
G | C | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-3485C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409567 | ||||||
chr2:69409683
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485-3601C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409683 | ||||||
chr2:69409824
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485-3742A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409824 | ||||||
chr2:69409948
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485-3866A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69409948 | ||||||
chr2:69410087
|
T | C | 100 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(97): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.485-4005A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410087 | ||||||
chr2:69410231
|
A | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-4149T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410231 | ||||||
chr2:69410303
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.485-4221G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410303 | ||||||
chr2:69410338
|
G | A | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.485-4256C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410338 | ||||||
chr2:69410684
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484+4501C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410684 | ||||||
chr2:69410696
|
C | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.484+4489G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410696 | ||||||
chr2:69410701
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.484+4484G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410701 | ||||||
chr2:69410832
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.484+4353G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69410832 | ||||||
chr2:69411029
|
G | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0137 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.484+4156C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411029 | ||||||
chr2:69411154
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.484+4031C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411154 | ||||||
chr2:69411306
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.484+3879G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411306 | ||||||
chr2:69411353
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.484+3832T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411353 | ||||||
chr2:69411568
|
T | G | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.484+3617A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411568 | ||||||
chr2:69411575
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.484+3610A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411575 | ||||||
chr2:69411599
|
A | T | 1 | a0001c0003t0001g0192 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.484+3586T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411599 | ||||||
chr2:69411774
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.484+3411G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411774 | ||||||
chr2:69411803
|
A | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+3382T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411803 | ||||||
chr2:69411891
|
C | G | 2 | a0002c0002t0001g0276a0002c0002t0001g0337 | 2 | NA18953.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.484+3294G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411891 | ||||||
chr2:69411915
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(245): Show | 253 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.484+3270A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411915 | ||||||
chr2:69411950
|
G | A | 9 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0112others(6): Show | 9 | NA18965.hp1 NA18966.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+3235C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411950 | ||||||
chr2:69412014
|
C | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 42 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.484+3171G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412014 | ||||||
chr2:69412083
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.484+3102C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412083 | ||||||
chr2:69412197
|
C | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+2988G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412197 | ||||||
chr2:69412423
|
G | T | 1 | a0001c0001t0001g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.484+2762C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412423 | ||||||
chr2:69412428
|
C | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0359a0001c0001t0001g0360 | 3 | HG02258.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.484+2757G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412428 | ||||||
chr2:69412458
|
C | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+2727G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412458 | ||||||
chr2:69412480
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.484+2705T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412480 | ||||||
chr2:69412491
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.484+2694T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412491 | ||||||
chr2:69412512
|
G | A | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.484+2673C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412512 | ||||||
chr2:69412534
|
G | A | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.484+2651C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412534 | ||||||
chr2:69412631
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.484+2554G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412631 | ||||||
chr2:69412718
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+2467G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412718 | ||||||
chr2:69412779
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(134): Show | 140 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.484+2406C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412779 | ||||||
chr2:69412857
|
C | CA | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(198): Show | 206 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.484+2327dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412857 | ||||||
chr2:69412875
|
G | A | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.484+2310C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412875 | ||||||
chr2:69412877
|
C | G | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.484+2308G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412877 | ||||||
chr2:69412881
|
T | C | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.484+2304A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412881 | ||||||
chr2:69412887
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.484+2298T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412887 | ||||||
chr2:69412949
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.484+2236T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412949 | ||||||
chr2:69413013
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.484+2172C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413013 | ||||||
chr2:69413057
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484+2128C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413057 | ||||||
chr2:69413115
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.484+2070A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413115 | ||||||
chr2:69413217
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 42 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.484+1968C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413217 | ||||||
chr2:69413238
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+1947A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413238 | ||||||
chr2:69413241
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+1944G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413241 | ||||||
chr2:69413246
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.484+1939A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413246 | ||||||
chr2:69413287
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.484+1898T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413287 | ||||||
chr2:69413304
|
A | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.484+1881T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413304 | ||||||
chr2:69413334
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(134): Show | 140 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.484+1851G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413334 | ||||||
chr2:69413338
|
T | TA | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.484+1846dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413338 | ||||||
chr2:69413404
|
G | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(245): Show | 253 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.484+1781C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413404 | ||||||
chr2:69413586
|
C | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0153others(32): Show | 37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.484+1599G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413586 | ||||||
chr2:69413590
|
C | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.484+1595G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413590 | ||||||
chr2:69413619
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484+1566G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413619 | ||||||
chr2:69413625
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+1560C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413625 | ||||||
chr2:69413634
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.484+1551G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413634 | ||||||
chr2:69413660
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.484+1525C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413660 | ||||||
chr2:69413664
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.484+1521A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413664 | ||||||
chr2:69413749
|
ACT | A | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.484+1434_484+1435d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413749 | ||||||
chr2:69413753
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+1432A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413753 | ||||||
chr2:69413770
|
C | T | 3 | a0001c0001t0001g0355a0001c0001t0001g0356a0002c0002t0001g0260 | 3 | HG02109.hp2 HG02717.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.484+1415G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413770 | ||||||
chr2:69413880
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.484+1305G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413880 | ||||||
chr2:69413919
|
C | T | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.484+1266G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413919 | ||||||
chr2:69414018
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.484+1167C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414018 | ||||||
chr2:69414223
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.484+962G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414223 | ||||||
chr2:69414234
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.484+951T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414234 | ||||||
chr2:69414392
|
G | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.484+793C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414392 | ||||||
chr2:69414618
|
T | TA | 18 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0152others(15): Show | 18 | HG00438.hp1 HG00735.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.484+566dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414618 | ||||||
chr2:69414618
|
TA | T | 79 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0040others(76): Show | 79 | HG00438.hp2 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.484+566delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414618 | ||||||
chr2:69414618
|
TAA | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 156 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.484+565_484+566del others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414618 | ||||||
chr2:69414671
|
T | C | 1 | a0002c0002t0001g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+514A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414671 | ||||||
chr2:69414741
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.484+444C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414741 | ||||||
chr2:69414932
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.484+253A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414932 | ||||||
chr2:69414936
|
A | G | 2 | a0002c0002t0001g0285a0002c0002t0001g0286 | 2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.484+249T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414936 | ||||||
chr2:69414994
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.484+191C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414994 | ||||||
chr2:69415004
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.484+181C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69415004 | ||||||
chr2:69415059
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+126C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69415059 | ||||||
chr2:69415381
|
C | CT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(99): Show | 104 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.370-83dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415381 | ||||||
chr2:69415440
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(241): Show | 249 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.370-141A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415440 | ||||||
chr2:69415483
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.370-184C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415483 | ||||||
chr2:69415554
|
A | T | 1 | a0001c0001t0001g0233 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.370-255T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415554 | ||||||
chr2:69415703
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.370-404G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415703 | ||||||
chr2:69415778
|
C | A | 1 | a0002c0002t0001g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.370-479G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415778 | ||||||
chr2:69415838
|
G | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(245): Show | 253 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.370-539C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415838 | ||||||
chr2:69415968
|
AT | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-670delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415968 | ||||||
chr2:69415991
|
A | AG | 138 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0051others(135): Show | 141 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.370-693dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415991 | ||||||
chr2:69416287
|
T | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0282a0002c0002t0001g0283others(1): Show | 4 | NA18953.hp2 NA18955.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-988A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416287 | ||||||
chr2:69416293
|
TTAA | T | 4 | a0002c0002t0001g0257a0002c0002t0001g0322a0002c0002t0001g0323others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-997_370-995del others(3): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416293 | ||||||
chr2:69416316
|
AATT | A | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.370-1020_370-1018d others(5): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416316 | ||||||
chr2:69416374
|
A | ATAT | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(142): Show | 147 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.370-1078_370-1076d others(5): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416374 | ||||||
chr2:69416511
|
TA | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0063others(31): Show | 34 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(31): Show |
intron_variant | MODIFIER | c.370-1213delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416511 | ||||||
chr2:69416634
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.370-1335T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416634 | ||||||
chr2:69416716
|
T | G | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.370-1417A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416716 | ||||||
chr2:69416820
|
C | T | 104 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(101): Show | 107 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.370-1521G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416820 | ||||||
chr2:69416853
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.370-1554C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416853 | ||||||
chr2:69416909
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.370-1610T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69416909 | ||||||
chr2:69417361
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.370-2062C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417361 | ||||||
chr2:69417369
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG00735.hp1 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.370-2070C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417369 | ||||||
chr2:69417409
|
G | A | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-2110C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417409 | ||||||
chr2:69417490
|
AAT | A | 46 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0069others(43): Show | 46 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.369+2046_369+2047d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417490 | ||||||
chr2:69417491
|
AT | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(65): Show | 70 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.369+2046delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417491 | ||||||
chr2:69417492
|
T | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0050others(128): Show | 134 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.369+2046A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417492 | ||||||
chr2:69417567
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.369+1971C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417567 | ||||||
chr2:69417771
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.369+1767C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417771 | ||||||
chr2:69417778
|
C | A | 6 | a0002c0002t0001g0325a0002c0002t0001g0333a0002c0002t0001g0334others(3): Show | 6 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1760G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417778 | ||||||
chr2:69417856
|
G | GA | 13 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(10): Show | 14 | HG01243.hp1 HG02257.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.369+1681dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417856 | ||||||
chr2:69417934
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.369+1604G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69417934 | ||||||
chr2:69418023
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0119 | 2 | NA18966.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.369+1515C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418023 | ||||||
chr2:69418113
|
T | TG | 134 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0050others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+1424dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418113 | ||||||
chr2:69418217
|
T | G | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.369+1321A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418217 | ||||||
chr2:69418236
|
C | CA | 4 | a0001c0001t0001g0139a0001c0001t0001g0352a0001c0001t0001g0355others(1): Show | 4 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1301dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418236 | ||||||
chr2:69418290
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.369+1248G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418290 | ||||||
chr2:69418306
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01168.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.369+1232C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418306 | ||||||
chr2:69418318
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.369+1220A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418318 | ||||||
chr2:69418362
|
TG | T | 7 | a0001c0003t0001g0105a0001c0003t0001g0173a0001c0003t0001g0184others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+1175delC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418362 | ||||||
chr2:69418387
|
A | C | 1 | a0002c0002t0001g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.369+1151T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418387 | ||||||
chr2:69418422
|
A | C | 1 | a0002c0002t0001g0303 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.369+1116T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418422 | ||||||
chr2:69418560
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+978C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418560 | ||||||
chr2:69418611
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.369+927G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418611 | ||||||
chr2:69418628
|
G | A | 39 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(36): Show | 39 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.369+910C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418628 | ||||||
chr2:69418633
|
C | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.369+905G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418633 | ||||||
chr2:69418696
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.369+842G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418696 | ||||||
chr2:69418716
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.369+822T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418716 | ||||||
chr2:69418841
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00621.hp2 HG02015.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+697T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418841 | ||||||
chr2:69418985
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.369+553G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418985 | ||||||
chr2:69419022
|
T | C | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+516A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419022 | ||||||
chr2:69419041
|
G | GTGGTGGC others(3): Show |
1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.369+487_369+496dup others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419041 | ||||||
chr2:69419104
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.369+434C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419104 | ||||||
chr2:69419186
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0201 | 2 | NA18956.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.369+352G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419186 | ||||||
chr2:69419214
|
CG | C | 133 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0050others(130): Show | 136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+323delC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419214 | ||||||
chr2:69419214
|
CGG | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(103): Show | 108 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.369+322_369+323del others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419214 | ||||||
chr2:69419225
|
G | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.369+313C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419225 | ||||||
chr2:69419358
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG01891.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.369+180T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419358 | ||||||
chr2:69419372
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.369+166C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419372 | ||||||
chr2:69419409
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.369+129C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419409 | ||||||
chr2:69419818
|
C | T | 98 | a0001c0001t0001g0060a0002c0002t0001g0001a0002c0002t0001g0006others(95): Show | 101 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.303-214G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69419818 | ||||||
chr2:69419881
|
A | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.303-277T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69419881 | ||||||
chr2:69419921
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.303-317T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69419921 | ||||||
chr2:69419987
|
G | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.303-383C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69419987 | ||||||
chr2:69420003
|
AT | A | 133 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(130): Show | 136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.303-400delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420003 | ||||||
chr2:69420016
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.303-412A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420016 | ||||||
chr2:69420109
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.303-505T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420109 | ||||||
chr2:69420145
|
A | G | 40 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(37): Show | 40 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.303-541T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420145 | ||||||
chr2:69420394
|
T | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-790A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420394 | ||||||
chr2:69420515
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.303-911C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420515 | ||||||
chr2:69420603
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0208 | 2 | NA18954.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.303-999A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420603 | ||||||
chr2:69420984
|
A | T | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.303-1380T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420984 | ||||||
chr2:69420986
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.303-1382A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420986 | ||||||
chr2:69421051
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.303-1447C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421051 | ||||||
chr2:69421192
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.303-1588T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421192 | ||||||
chr2:69421305
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.303-1701G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421305 | ||||||
chr2:69421388
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.303-1784G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421388 | ||||||
chr2:69421409
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.303-1805C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421409 | ||||||
chr2:69421420
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.303-1816G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421420 | ||||||
chr2:69421535
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG00735.hp1 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.303-1931A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421535 | ||||||
chr2:69421562
|
C | CT | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(141): Show | 148 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.303-1959dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421562 | ||||||
chr2:69421562
|
C | CTT | 46 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(43): Show | 47 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.303-1960_303-1959d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421562 | ||||||
chr2:69421562
|
C | CTTT | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(4): Show | 7 | HG00621.hp2 NA18943.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-1961_303-1959d others(5): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421562 | ||||||
chr2:69421562
|
CT | C | 47 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(44): Show | 47 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.303-1959delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421562 | ||||||
chr2:69421603
|
T | C | 1 | a0002c0002t0001g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302+1979A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421603 | ||||||
chr2:69421660
|
C | T | 1 | a0003c0004t0001g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.302+1922G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421660 | ||||||
chr2:69421661
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+1921C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421661 | ||||||
chr2:69421697
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 109 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.302+1885C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421697 | ||||||
chr2:69421735
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.302+1847A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421735 | ||||||
chr2:69421852
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.302+1730C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421852 | ||||||
chr2:69422086
|
AATATGCC others(11): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.302+1478_302+1495d others(20): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422086 | ||||||
chr2:69422406
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.302+1176C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422406 | ||||||
chr2:69422614
|
AT | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.302+967delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422614 | ||||||
chr2:69422836
|
C | A | 38 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(35): Show | 38 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.302+746G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422836 | ||||||
chr2:69422952
|
G | T | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.302+630C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422952 | ||||||
chr2:69422986
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.302+596C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422986 | ||||||
chr2:69423080
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302+502C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423080 | ||||||
chr2:69423146
|
T | TTG | 6 | a0001c0001t0001g0139a0001c0001t0001g0197a0001c0001t0001g0353others(3): Show | 6 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+434_302+435dup others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423146 | ||||||
chr2:69423146
|
TTGTGTGT others(44): Show |
T | 35 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(32): Show | 35 | HG00323.hp2 HG00558.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.302+385_302+435del others(51): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423146 | ||||||
chr2:69423158
|
GTGTGTGT others(43): Show |
G | 3 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0090 | 3 | HG00642.hp1 HG01175.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.302+374_302+423del others(50): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423158 | ||||||
chr2:69423166
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.302+416C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423166 | ||||||
chr2:69423168
|
A | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 207 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.302+414T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423168 | ||||||
chr2:69423170
|
G | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.302+412C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423170 | ||||||
chr2:69423170
|
G | GTA | 61 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 62 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.302+411_302+412ins others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423170 | ||||||
chr2:69423170
|
G | GTGTA | 6 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 7 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.302+411_302+412ins others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423170 | ||||||
chr2:69423206
|
T | TG | 14 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(11): Show | 14 | HG00544.hp1 HG00642.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+375dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423206 | ||||||
chr2:69423207
|
GT | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0359a0001c0001t0001g0360others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+374delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423207 | ||||||
chr2:69423208
|
T | G | 23 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(20): Show | 23 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.302+374A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423208 | ||||||
chr2:69423208
|
T | TG | 103 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 107 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.302+373dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423208 | ||||||
chr2:69423208
|
T | TGG | 58 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0026others(55): Show | 58 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.302+372_302+373dup others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423208 | ||||||
chr2:69423236
|
CTGTGTGA others(3): Show |
C | 7 | a0001c0001t0001g0015a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+336_302+345del others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(5): Show |
C | 7 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0049others(4): Show | 7 | HG00597.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+334_302+345del others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(7): Show |
C | 45 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(42): Show | 46 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.302+332_302+345del others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(9): Show |
C | 36 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0059others(33): Show | 37 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.302+330_302+345del others(16): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(11): Show |
C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.302+328_302+345del others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(13): Show |
C | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+326_302+345del others(20): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423236
|
CTGTGTGA others(19): Show |
C | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302+320_302+345del others(26): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423236 | ||||||
chr2:69423243
|
A | AGT | 31 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0150others(28): Show | 32 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.302+337_302+338dup others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
A | AGTGT | 14 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(11): Show | 14 | HG01106.hp1 HG02027.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+335_302+338dup others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGT | A | 15 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0166others(12): Show | 15 | HG00621.hp1 HG00673.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.302+337_302+338del others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGTGT | A | 10 | a0001c0001t0001g0139a0001c0001t0001g0161a0001c0001t0001g0164others(7): Show | 10 | HG00735.hp1 HG02109.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+335_302+338del others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGTGTGT | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0219a0001c0001t0001g0352others(1): Show | 4 | HG01069.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+333_302+338del others(6): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGTGTGTG others(7): Show |
A | 14 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(11): Show | 14 | HG00408.hp2 HG02015.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+325_302+338del others(14): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGTGTGTG others(9): Show |
A | 112 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(109): Show | 115 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.302+323_302+338del others(16): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423243
|
AGTGTGTG others(11): Show |
A | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+321_302+338del others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423243 | ||||||
chr2:69423247
|
T | A | 1 | a0003c0004t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.302+335A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423247 | ||||||
chr2:69423249
|
T | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+333A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423249 | ||||||
chr2:69423251
|
T | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0049others(6): Show | 9 | HG00597.hp2 HG02559.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+331A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423251 | ||||||
chr2:69423253
|
T | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(42): Show | 46 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.302+329A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423253 | ||||||
chr2:69423255
|
T | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0059others(33): Show | 37 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.302+327A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423255 | ||||||
chr2:69423257
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.302+325A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423257 | ||||||
chr2:69423259
|
T | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+323A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423259 | ||||||
chr2:69423265
|
T | A | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302+317A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423265 | ||||||
chr2:69423274
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+308C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423274 | ||||||
chr2:69423290
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.302+292T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423290 | ||||||
chr2:69423313
|
T | A | 38 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(35): Show | 38 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.302+269A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423313 | ||||||
chr2:69423395
|
C | T | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.302+187G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423395 | ||||||
chr2:69423422
|
A | AT | 133 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(130): Show | 136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.302+159dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423422 | ||||||
chr2:69423741
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.167-24C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69423741 | ||||||
chr2:69423845
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-128C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69423845 | ||||||
chr2:69423897
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.167-180C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69423897 | ||||||
chr2:69423978
|
G | C | 4 | a0002c0002t0001g0263a0002c0002t0001g0280a0002c0002t0001g0281others(1): Show | 4 | HG01109.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-261C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69423978 | ||||||
chr2:69424144
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.167-427G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424144 | ||||||
chr2:69424164
|
C | G | 4 | a0002c0002t0001g0333a0002c0002t0001g0334a0002c0002t0001g0357others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-447G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424164 | ||||||
chr2:69424166
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0063others(31): Show | 34 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(31): Show |
intron_variant | MODIFIER | c.167-449C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424166 | ||||||
chr2:69424170
|
C | CA | 26 | a0001c0001t0001g0054a0001c0001t0001g0104a0001c0001t0001g0150others(23): Show | 26 | HG00639.hp1 HG00673.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.167-454dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424170
|
CA | C | 6 | a0001c0001t0001g0167a0001c0001t0001g0252a0002c0002t0001g0254others(3): Show | 6 | HG01106.hp2 HG01109.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.167-454delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424170
|
CAA | C | 36 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(33): Show | 36 | HG00558.hp1 HG00642.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.167-455_167-454del others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424170
|
CAAA | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0074others(8): Show | 11 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.167-456_167-454del others(3): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424170
|
CAAAA | C | 37 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(34): Show | 37 | HG00741.hp1 HG01884.hp2 HG02004.hp1 others(34): Show |
intron_variant | MODIFIER | c.167-457_167-454del others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424170
|
CAAAAA | C | 31 | a0001c0001t0001g0061a0001c0001t0001g0106a0001c0001t0001g0107others(28): Show | 31 | HG02074.hp1 HG02559.hp2 HG02572.hp1 others(28): Show |
intron_variant | MODIFIER | c.167-458_167-454del others(5): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424170 | ||||||
chr2:69424190
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.167-483_167-474del others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424190 | ||||||
chr2:69424194
|
A | T | 4 | a0003c0004t0001g0142a0003c0004t0001g0143a0003c0004t0001g0144others(1): Show | 4 | HG01243.hp1 HG06807.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-477T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424194 | ||||||
chr2:69424195
|
A | T | 1 | a0002c0002t0001g0254 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.167-478T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424195 | ||||||
chr2:69424196
|
A | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0103others(8): Show | 11 | HG00597.hp2 HG00735.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.167-479T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424196 | ||||||
chr2:69424196
|
AAAAT | A | 36 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0260others(33): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.167-483_167-480del others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424196 | ||||||
chr2:69424198
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0348 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(29): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.167-482_167-481ins others(18): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(26): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(11): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(11): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAATAT others(16): Show |
1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(23): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAAATAT others(20): Show |
1 | a0001c0001t0001g0101 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(27): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAATATA others(3): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0356 | 2 | HG00609.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.167-482_167-481ins others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.167-482_167-481ins others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAAATATA others(19): Show |
1 | a0001c0001t0001g0100 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(26): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAATATAT others(4): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | HG02015.hp2 HG04184.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.167-482_167-481ins others(11): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | AAATATAT others(10): Show |
1 | a0001c0001t0001g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.167-482_167-481ins others(17): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0354 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.167-482_167-481ins others(15): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424198
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(61): Show | 65 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.167-481T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424198 | ||||||
chr2:69424199
|
A | AAAATATA others(6): Show |
1 | a0001c0001t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.167-483_167-482ins others(13): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424199 | ||||||
chr2:69424199
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0011 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.167-483_167-482ins others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424199 | ||||||
chr2:69424199
|
AT | A | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01074.hp2 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-483delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424199 | ||||||
chr2:69424200
|
T | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0045others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.167-483A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424200 | ||||||
chr2:69424201
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.167-485_167-484ins others(12): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424201 | ||||||
chr2:69424201
|
A | ATATATAT others(3): Show |
30 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(27): Show | 31 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.167-485_167-484ins others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424201 | ||||||
chr2:69424201
|
A | ATATGTAT others(3): Show |
1 | a0001c0001t0001g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.167-485_167-484ins others(10): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424201 | ||||||
chr2:69424201
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG00609.hp1 HG02015.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.167-484T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424201 | ||||||
chr2:69424202
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | HG00323.hp1 HG02165.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-485A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424202 | ||||||
chr2:69424217
|
A | ATCTCTCT others(1): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.167-501_167-500ins others(8): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424217 | ||||||
chr2:69424217
|
A | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0353a0003c0004t0001g0141others(4): Show | 7 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-500T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424217 | ||||||
chr2:69424219
|
A | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0033others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.167-502T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424219 | ||||||
chr2:69424262
|
G | A | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.167-545C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424262 | ||||||
chr2:69424344
|
A | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 50 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.167-627T>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424344 | ||||||
chr2:69424349
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.167-632G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424349 | ||||||
chr2:69424811
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.167-1094A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424811 | ||||||
chr2:69424878
|
C | CT | 194 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(191): Show | 197 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.167-1162dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424878 | ||||||
chr2:69424878
|
C | CTT | 35 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0069others(32): Show | 36 | HG01255.hp1 HG01516.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.167-1163_167-1162d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424878 | ||||||
chr2:69424910
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.167-1193A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424910 | ||||||
chr2:69425061
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.167-1344C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425061 | ||||||
chr2:69425145
|
T | A | 1 | a0002c0002t0001g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.167-1428A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425145 | ||||||
chr2:69425327
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.167-1610G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425327 | ||||||
chr2:69425358
|
AT | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 243 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.167-1642delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425358 | ||||||
chr2:69425505
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.167-1788G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425505 | ||||||
chr2:69425569
|
G | A | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167-1852C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425569 | ||||||
chr2:69425608
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.167-1891C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425608 | ||||||
chr2:69425635
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.167-1918C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425635 | ||||||
chr2:69426173
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.167-2456A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426173 | ||||||
chr2:69426209
|
C | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.167-2492G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426209 | ||||||
chr2:69426219
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.167-2502C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426219 | ||||||
chr2:69426344
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.167-2627C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426344 | ||||||
chr2:69426360
|
A | G | 1 | a0001c0001t0001g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.167-2643T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426360 | ||||||
chr2:69426369
|
T | G | 1 | a0002c0002t0001g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.167-2652A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426369 | ||||||
chr2:69426486
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.167-2769T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426486 | ||||||
chr2:69426532
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.167-2815A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426532 | ||||||
chr2:69426720
|
G | A | 12 | a0002c0002t0001g0257a0002c0002t0001g0321a0002c0002t0001g0322others(9): Show | 12 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.167-3003C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426720 | ||||||
chr2:69426984
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 5 | HG01167.hp2 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-3267C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69426984 | ||||||
chr2:69427067
|
AAAAAG | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 51 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.167-3355_167-3351d others(7): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427067 | ||||||
chr2:69427068
|
AAAAG | A | 181 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0050others(178): Show | 185 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.167-3355_167-3352d others(6): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427068 | ||||||
chr2:69427180
|
G | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.167-3463C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427180 | ||||||
chr2:69427242
|
G | A | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-3525C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427242 | ||||||
chr2:69427249
|
G | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.167-3532C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427249 | ||||||
chr2:69427254
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.167-3537T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427254 | ||||||
chr2:69427401
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.167-3684C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427401 | ||||||
chr2:69427419
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.167-3702G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427419 | ||||||
chr2:69427679
|
C | CA | 63 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 64 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.167-3963dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427679 | ||||||
chr2:69427679
|
C | CAA | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG00609.hp1 HG01928.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.167-3964_167-3963d others(4): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427679 | ||||||
chr2:69427679
|
CA | C | 47 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0064others(44): Show | 47 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.167-3963delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427679 | ||||||
chr2:69427795
|
A | C | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-4078T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427795 | ||||||
chr2:69427811
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166+4091C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427811 | ||||||
chr2:69427979
|
C | A | 20 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(17): Show | 20 | HG02074.hp1 HG02451.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.166+3923G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427979 | ||||||
chr2:69427997
|
T | G | 5 | a0001c0001t0001g0139a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+3905A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427997 | ||||||
chr2:69428009
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166+3893G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428009 | ||||||
chr2:69428035
|
G | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+3867C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428035 | ||||||
chr2:69428145
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.166+3757G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428145 | ||||||
chr2:69428362
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.166+3540A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428362 | ||||||
chr2:69428403
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+3499G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428403 | ||||||
chr2:69428413
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.166+3489A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428413 | ||||||
chr2:69428658
|
T | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0060others(131): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.166+3244A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428658 | ||||||
chr2:69428690
|
A | C | 1 | a0002c0002t0001g0261 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.166+3212T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428690 | ||||||
chr2:69428946
|
A | G | 1 | a0003c0004t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.166+2956T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69428946 | ||||||
chr2:69429049
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0044 | 2 | NA18973.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.166+2853A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429049 | ||||||
chr2:69429145
|
T | C | 7 | a0002c0002t0001g0260a0002c0002t0001g0328a0002c0002t0001g0329others(4): Show | 7 | NA18946.hp1 NA18969.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.166+2757A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429145 | ||||||
chr2:69429222
|
T | C | 36 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(33): Show | 36 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.166+2680A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429222 | ||||||
chr2:69429226
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.166+2676A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429226 | ||||||
chr2:69429345
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.166+2557G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429345 | ||||||
chr2:69429370
|
C | G | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+2532G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429370 | ||||||
chr2:69429392
|
T | C | 5 | a0002c0002t0001g0333a0002c0002t0001g0334a0002c0002t0001g0335others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+2510A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429392 | ||||||
chr2:69429889
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.166+2013A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69429889 | ||||||
chr2:69430047
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0062 | 2 | HG01433.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.166+1855T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430047 | ||||||
chr2:69430217
|
CT | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(234): Show | 242 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.166+1684delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430217 | ||||||
chr2:69430352
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.166+1550T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430352 | ||||||
chr2:69430417
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.166+1485A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430417 | ||||||
chr2:69430437
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.166+1465G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430437 | ||||||
chr2:69430461
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.166+1441G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430461 | ||||||
chr2:69430626
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.166+1276C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430626 | ||||||
chr2:69430713
|
T | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.166+1189A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430713 | ||||||
chr2:69430837
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.166+1065G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430837 | ||||||
chr2:69430870
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0044 | 2 | NA18973.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.166+1032C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430870 | ||||||
chr2:69430904
|
G | A | 1 | a0002c0002t0001g0337 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.166+998C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430904 | ||||||
chr2:69430922
|
G | T | 1 | a0002c0002t0001g0337 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.166+980C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430922 | ||||||
chr2:69431092
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG02071.hp2 HG02083.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+810C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69431092 | ||||||
chr2:69431392
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.166+510T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69431392 | ||||||
chr2:69431454
|
C | T | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+448G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69431454 | ||||||
chr2:69431636
|
T | A | 1 | a0002c0002t0001g0341 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.166+266A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69431636 | ||||||
chr2:69431753
|
T | C | 1 | a0002c0002t0001g0336 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.166+149A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69431753 | ||||||
chr2:69432129
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.63-124A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432129 | ||||||
chr2:69432264
|
A | G | 1 | a0002c0002t0001g0260 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.63-259T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432264 | ||||||
chr2:69432270
|
T | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0050others(134): Show | 141 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.63-265A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432270 | ||||||
chr2:69432312
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.63-307G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432312 | ||||||
chr2:69432313
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.63-308C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432313 | ||||||
chr2:69432357
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.63-352C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432357 | ||||||
chr2:69432392
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-387A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432392 | ||||||
chr2:69432780
|
T | TACC | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.63-776_63-775insGG others(1): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432780 | ||||||
chr2:69432874
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG02976.hp2 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-869C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432874 | ||||||
chr2:69432972
|
C | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.63-967G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432972 | ||||||
chr2:69432999
|
A | C | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.63-994T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69432999 | ||||||
chr2:69433082
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.63-1077C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433082 | ||||||
chr2:69433085
|
GGTTGCAG others(12): Show |
G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(237): Show | 245 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.63-1099_63-1081del others(19): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433085 | ||||||
chr2:69433116
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0002g0361 | 2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.63-1111G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433116 | ||||||
chr2:69433124
|
TG | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-1120delC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433124 | ||||||
chr2:69433150
|
C | CA | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 176 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.63-1146dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433150 | ||||||
chr2:69433150
|
C | CAA | 16 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG00621.hp2 HG01106.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.63-1147_63-1146dup others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433150 | ||||||
chr2:69433203
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.63-1198C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433203 | ||||||
chr2:69433215
|
T | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.63-1210A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433215 | ||||||
chr2:69433432
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG01884.hp1 HG02818.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-1427C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433432 | ||||||
chr2:69433481
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63-1476C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433481 | ||||||
chr2:69433493
|
T | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.63-1488A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433493 | ||||||
chr2:69433514
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.63-1509G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433514 | ||||||
chr2:69433529
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63-1524C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433529 | ||||||
chr2:69433538
|
C | T | 5 | a0003c0004t0001g0141a0003c0004t0001g0142a0003c0004t0001g0143others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.63-1533G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433538 | ||||||
chr2:69433568
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-1563A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433568 | ||||||
chr2:69433610
|
G | A | 1 | a0002c0002t0001g0341 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.63-1605C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433610 | ||||||
chr2:69433709
|
A | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.63-1704T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433709 | ||||||
chr2:69433748
|
T | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.63-1743A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433748 | ||||||
chr2:69433772
|
C | T | 4 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-1767G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433772 | ||||||
chr2:69433940
|
G | GT | 36 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0069others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.63-1936dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433940 | ||||||
chr2:69433940
|
GT | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(156): Show | 164 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.63-1936delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433940 | ||||||
chr2:69433940
|
GTT | G | 42 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0061others(39): Show | 42 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(39): Show |
intron_variant | MODIFIER | c.63-1937_63-1936del others(2): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433940 | ||||||
chr2:69434063
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0361 | 2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.63-2058C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434063 | ||||||
chr2:69434149
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.63-2144G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434149 | ||||||
chr2:69434150
|
T | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 247 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.63-2145A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434150 | ||||||
chr2:69434208
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63-2203C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434208 | ||||||
chr2:69434668
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(243): Show | 251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.63-2663T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434668 | ||||||
chr2:69434747
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.62+2614G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434747 | ||||||
chr2:69434836
|
T | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | NA18612.hp1 NA18939.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+2525A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434836 | ||||||
chr2:69434864
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.62+2497C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434864 | ||||||
chr2:69434987
|
A | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(28): Show | 31 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.62+2374T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434987 | ||||||
chr2:69435072
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.62+2289C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435072 | ||||||
chr2:69435109
|
C | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.62+2252G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435109 | ||||||
chr2:69435283
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.62+2078C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435283 | ||||||
chr2:69435485
|
A | C | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.62+1876T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435485 | ||||||
chr2:69435565
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.62+1796A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435565 | ||||||
chr2:69435589
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0106others(26): Show | 29 | HG01243.hp2 HG02074.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.62+1772T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435589 | ||||||
chr2:69435594
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.62+1767C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435594 | ||||||
chr2:69435916
|
C | CT | 46 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0059others(43): Show | 47 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.62+1444dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435916 | ||||||
chr2:69435916
|
CT | C | 7 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(4): Show | 7 | HG01168.hp1 HG01516.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.62+1444delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435916 | ||||||
chr2:69435980
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62+1381G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435980 | ||||||
chr2:69435987
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.62+1374C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69435987 | ||||||
chr2:69436064
|
A | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+1297T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436064 | ||||||
chr2:69436146
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.62+1215A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436146 | ||||||
chr2:69436148
|
T | G | 1 | a0001c0001t0001g0253 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.62+1213A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436148 | ||||||
chr2:69436149
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.62+1212A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436149 | ||||||
chr2:69436173
|
G | A | 100 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0002g0361others(97): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.62+1188C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436173 | ||||||
chr2:69436195
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62+1166T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436195 | ||||||
chr2:69436455
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.62+906C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436455 | ||||||
chr2:69436537
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.62+824T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436537 | ||||||
chr2:69436577
|
G | A | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.62+784C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436577 | ||||||
chr2:69436654
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62+707T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436654 | ||||||
chr2:69436666
|
T | G | 1 | a0001c0001t0001g0351 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.62+695A>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436666 | ||||||
chr2:69436705
|
G | C | 1 | a0001c0001t0001g0352 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.62+656C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436705 | ||||||
chr2:69436927
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0002g0361 | 2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.62+434A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436927 | ||||||
chr2:69436942
|
G | A | 4 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+419C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69436942 | ||||||
chr2:69437013
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.62+348G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437013 | ||||||
chr2:69437197
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.62+164G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437197 | ||||||
chr2:69437200
|
A | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02451.hp1 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62+161T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437200 | ||||||
chr2:69437229
|
C | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | NA18971.hp2 NA18994.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+132G>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437229 | ||||||
chr2:69437281
|
A | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 47 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.62+80T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437281 | ||||||
chr2:69437332
|
C | A | 2 | a0002c0002t0001g0357a0002c0002t0001g0358 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.62+29G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437332 | ||||||
chr2:69437352
|
G | A | 2 | a0001c0001t0001g0359a0001c0001t0001g0360 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.62+9C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437352 |