Item | Value |
---|---|
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 | MAATA others(249): Show |
chr2 | 69391126 | 69442435 |
a0002 | 0/1 | 254 | 100 | 25 | 19 | 41 | 4 | 10 | 30 | NFU1_chr2_69391126_69442435 | NFU1 | MAATA others(249): Show |
chr2 | 69391126 | 69442435 |
a0003 | 0/0 | 254 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | MAATA others(249): Show |
chr2 | 69391126 | 69442435 |
a0004 | 0/0 | 254 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | MAATA others(249): Show |
chr2 | 69391126 | 69442435 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 762 | 250 | 63 | 29 | 131 | 5 | 21 | NFU1_chr2_69391126_69442435 | NFU1 | ATGGC others(757): Show |
chr2 | 69391126 | 69442435 | ||
a0001c0003 | 0/0 | 762 | 9 | 0 | 9 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | ATGGC others(757): Show |
chr2 | 69391126 | 69442435 | ||
a0002c0002 | 0/1 | 762 | 100 | 25 | 19 | 41 | 4 | 10 | NFU1_chr2_69391126_69442435 | NFU1 | ATGGC others(757): Show |
chr2 | 69391126 | 69442435 | ||
a0003c0004 | 0/0 | 762 | 5 | 4 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | ATGGC others(757): Show |
chr2 | 69391126 | 69442435 | ||
a0004c0005 | 0/0 | 762 | 4 | 0 | 2 | 0 | 1 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | ATGGC others(757): Show |
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 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
a0001c0001t0002 | 0/0 | 898 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
a0001c0003t0001 | 0/0 | 898 | 9 | 0 | 9 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
a0002c0002t0001 | 0/1 | 898 | 100 | 25 | 19 | 41 | 4 | 10 | NFU1_chr2_69391126_69442435 | NFU1 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
a0003c0004t0001 | 0/0 | 898 | 5 | 4 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
a0004c0005t0001 | 0/0 | 898 | 4 | 0 | 2 | 0 | 1 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | ACTCC others(893): Show |
chr2 | 69391126 | 69442435 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0004 | 1/0 | 3 | 0 | 1 | 1 | 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 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0198 | 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 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0212 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0001 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0307 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0002c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0003c0004t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
a0004c0005t0001g0107 | 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 | g0228 | EUR | GBR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0288 | EUR | GBR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | CHS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01106 | hp2 | a0004 | c0005 | t0001 | g0107 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0306 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0325 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01243 | hp1 | a0003 | c0004 | t0001 | g0154 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0216 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0252 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0326 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01516 | hp2 | a0004 | c0005 | t0001 | g0080 | EUR | IBS | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0301 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0182 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0229 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01981 | hp1 | a0004 | c0005 | t0001 | g0102 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | CDX | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0339 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0338 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0150 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0276 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0317 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | PJL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03927 | hp2 | a0004 | c0005 | t0001 | g0103 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0320 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0303 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0152 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0275 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ASW | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ASW | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0097 | 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 | g0322 | SAS | GIH | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | GIH | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0280 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
HG06807 | hp2 | a0003 | c0004 | t0001 | g0153 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA21309 | hp1 | a0003 | c0004 | t0001 | g0151 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0307 | REF | REF | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | NFU1_chr2_69391126_69442435 | NFU1 | chr2 | 69391126 | 69442435 |
view | 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 | 99 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(96): 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 |
view | 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 |
view | 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 |
view | 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 | a0002c0002t0001g0323 | 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 | a0003c0004t0001g0151 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0002c0002t0001g0278 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0002c0002t0001g0294 | 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(243): 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 | a0002c0002t0001g0312 | 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.721-683T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69396973 | |||||||
chr2:69397045 | A | G | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): 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 | a0001c0001t0001g0007 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0113 | 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 | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
247 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(244): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0194 | 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 | 124 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(121): Show |
135 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(132): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0059 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 149 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
161 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(158): 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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
222 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.721-1328A>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397618 | |||||||
chr2:69397618 | T | TA | 22 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(19): 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 | a0001c0001t0001g0063 a0003c0004t0001g0150 a0003c0004t0001g0151 others(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 | a0001c0001t0001g0148 | 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 | a0002c0002t0001g0290 | 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 | 229 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
243 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.721-1579T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69397869 | |||||||
chr2:69397914 | CA | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(45): 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 | 141 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(138): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(150): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0147 | 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 | 229 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
243 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(240): 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0003c0004t0001g0150 | 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 | a0002c0002t0001g0249 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0226 |
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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0217 a0001c0001t0001g0230 others(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 | 21 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0032 others(18): 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 | a0001c0001t0001g0122 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0002c0002t0001g0322 | 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0003c0004t0001g0151 a0003c0004t0001g0154 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0002c0002t0001g0255 a0002c0002t0001g0320 a0002c0002t0001g0322 |
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 | 222 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
236 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.720+487delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 7/7 | chr2 | 69399876 | |||||||
chr2:69399933 | C | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0335 | 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 | 126 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(123): Show |
137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.546-168dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69400705 | |||||||
chr2:69400744 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0117 | 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 | a0002c0002t0001g0263 a0002c0002t0001g0274 a0002c0002t0001g0292 |
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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | 128 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(125): Show |
139 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.546-930A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69401468 | |||||||
chr2:69401898 | CT | C | 127 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(124): Show |
138 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.546-1361delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69401898 | |||||||
chr2:69402013 | A | C | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.546-1475T>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69402013 | |||||||
chr2:69402421 | A | G | 237 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
251 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(248): 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0002c0002t0001g0270 a0002c0002t0001g0318 |
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 | a0001c0001t0001g0222 | 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 | 40 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(37): 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0148 | 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 | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(31): 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 | a0001c0001t0001g0203 | 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.545+2643C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69403379 | |||||||
chr2:69403427 | A | G | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0341 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0210 | 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 | a0002c0002t0001g0265 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0075 | 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0330 | 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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.545+1582A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404440 | |||||||
chr2:69404447 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0007 a0003c0004t0001g0150 a0003c0004t0001g0151 others(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 | a0002c0002t0001g0292 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0081 others(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 |
9 | a0001c0001t0001g0006 a0001c0001t0001g0082 a0001c0001t0001g0091 others(6): 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 | a0001c0001t0001g0329 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0330 a0003c0004t0001g0150 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0112 a0003c0004t0001g0153 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0111 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(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 |
35 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0041 others(32): Show |
43 | HG00597.hp1 HG00738.hp2 HG01069.hp2 others(40): 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 |
24 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0042 others(21): 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 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0133 a0002c0002t0001g0275 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0002c0002t0001g0262 others(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 | a0002c0002t0001g0263 a0002c0002t0001g0267 a0002c0002t0001g0270 others(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 |
5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0134 others(2): 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 | a0002c0002t0001g0314 | 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 | a0002c0002t0001g0338 a0002c0002t0001g0339 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | 24 | a0001c0001t0001g0008 a0001c0001t0001g0117 a0001c0001t0001g0118 others(21): 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 | a0001c0001t0001g0063 a0001c0001t0002g0342 |
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 | 89 | a0001c0001t0001g0073 a0002c0002t0001g0001 a0002c0002t0001g0014 others(86): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.545+1245C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 6/7 | chr2 | 69404777 | |||||||
chr2:69404797 | C | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0148 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): 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 | a0002c0002t0001g0294 | 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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0002c0002t0001g0288 | 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0002c0002t0001g0268 | 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0333 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.485-350dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406431 | |||||||
chr2:69406528 | A | G | 1 | a0001c0001t0001g0148 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.485-537C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69406619 | |||||||
chr2:69406629 | G | A | 1 | a0002c0002t0001g0018 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0053 |
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 | a0001c0001t0001g0333 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0334 | 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 | a0002c0002t0001g0260 | 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 | a0001c0001t0001g0007 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): 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 | a0001c0001t0001g0082 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0029 others(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 | 198 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(195): Show |
209 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(206): 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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0117 others(17): 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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0117 others(17): 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(243): 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0227 | 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 | 221 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
234 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.485-1931delT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408012 | |||||||
chr2:69408012 | CAA | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0072 | 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 | a0003c0004t0001g0150 | 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0212 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0210 | 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 | 53 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): 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 | 15 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0172 others(12): 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 | a0001c0001t0001g0031 a0001c0001t0001g0138 |
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 | 89 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(86): 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 | 130 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0068 others(127): Show |
141 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(138): 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0189 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0048 others(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 | 32 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0081 others(29): 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 | 94 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0057 others(91): Show |
105 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.485-2780delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69408861 | |||||||
chr2:69408885 | G | T | 1 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0001g0257 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0148 a0002c0002t0001g0273 |
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 | a0003c0004t0001g0150 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0073 | 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 | 92 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(89): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(99): 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0238 | 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.484+3832T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411353 | |||||||
chr2:69411568 | T | G | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0001c0001t0001g0335 | 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 | a0001c0003t0001g0174 | 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0001g0270 a0002c0002t0001g0318 |
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 | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.484+3270A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69411915 | |||||||
chr2:69411950 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0119 a0001c0001t0001g0121 others(5): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0336 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0340 a0001c0001t0001g0341 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0335 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 128 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(125): Show |
139 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.484+2406C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412779 | |||||||
chr2:69412857 | C | CA | 192 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(189): Show |
205 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.484+2327dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69412857 | |||||||
chr2:69412875 | G | A | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0050 | 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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0333 | 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 128 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(125): Show |
139 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.484+1851G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413334 | |||||||
chr2:69413338 | T | TA | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.484+1846dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413338 | |||||||
chr2:69413404 | G | T | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.484+1781C>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69413404 | |||||||
chr2:69413586 | C | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(30): 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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0194 | 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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0002c0002t0001g0253 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0148 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(247): Show |
intron_variant | MODIFIER | c.484+951T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 5/7 | chr2 | 69414234 | |||||||
chr2:69414392 | G | C | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(247): 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 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | 77 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(74): 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 | 143 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0021 others(140): Show |
155 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(152): 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 | a0002c0002t0001g0257 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0235 | 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 | a0002c0002t0001g0271 a0002c0002t0001g0273 |
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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): 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 | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
248 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.370-141A>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415440 | |||||||
chr2:69415483 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0035 | 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 | a0002c0002t0001g0270 | 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 | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | 129 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(126): Show |
140 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.370-693dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69415991 | |||||||
chr2:69416287 | T | C | 4 | a0002c0002t0001g0268 a0002c0002t0001g0269 a0002c0002t0001g0270 others(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 | a0002c0002t0001g0250 a0002c0002t0001g0302 a0002c0002t0001g0303 others(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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): 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 | 33 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0074 others(30): 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 | a0001c0001t0001g0075 | 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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | 96 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(93): Show |
106 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(103): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | 45 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0081 others(42): 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 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0021 others(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 | 122 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0022 others(119): Show |
133 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(130): 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0072 | 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 | a0002c0002t0001g0305 a0002c0002t0001g0314 a0002c0002t0001g0315 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+1424dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418113 | |||||||
chr2:69418217 | T | G | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0333 a0001c0001t0001g0335 others(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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0113 | 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 | 6 | a0001c0003t0001g0011 a0001c0003t0001g0116 a0001c0003t0001g0174 others(3): 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 | a0002c0002t0001g0288 | 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 | a0002c0002t0001g0284 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | 38 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): 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 | 229 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
243 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.369+905G>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69418633 | |||||||
chr2:69418696 | C | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0136 | 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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0160 a0001c0001t0001g0181 |
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 | 124 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0055 others(121): Show |
135 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.369+323delC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419214 | |||||||
chr2:69419214 | CGG | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.369+313C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 4/7 | chr2 | 69419225 | |||||||
chr2:69419358 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0133 a0001c0001t0001g0135 |
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 | 90 | a0001c0001t0001g0073 a0002c0002t0001g0001 a0002c0002t0001g0014 others(87): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0119 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.303-383C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69419987 | |||||||
chr2:69420003 | AT | A | 124 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(121): Show |
135 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.303-400delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420003 | |||||||
chr2:69420016 | T | C | 1 | a0001c0001t0001g0128 | 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.303-505T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69420109 | |||||||
chr2:69420145 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(36): 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 | a0001c0001t0001g0074 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0213 | 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(243): 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 | a0001c0001t0001g0333 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | 136 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
147 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.303-1959dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69421562 | |||||||
chr2:69421562 | C | CTT | 45 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0033 others(42): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0026 others(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 | 46 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0069 others(43): 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 | a0002c0002t0001g0278 | 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 | a0003c0004t0001g0152 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(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 | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0203 | 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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.302+967delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69422614 | |||||||
chr2:69422836 | C | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(34): 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 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0334 others(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 | 34 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(31): 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 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0245 | 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 | 193 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
206 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.302+414T>C | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423168 | |||||||
chr2:69423170 | G | A | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0340 a0001c0001t0001g0341 others(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 | 22 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(19): 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 | 101 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(98): Show |
106 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.302+373dupC | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423208 | |||||||
chr2:69423208 | T | TGG | 56 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0025 others(53): 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 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0071 others(32): 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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0003c0004t0001g0150 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0201 a0001c0001t0001g0333 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0120 others(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 | 105 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(102): Show |
114 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(111): 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0003c0004t0001g0153 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0071 others(32): 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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0003c0004t0001g0150 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0334 a0001c0001t0001g0335 others(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 | a0001c0001t0001g0173 | 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 | 37 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(34): 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.302+187G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423395 | |||||||
chr2:69423422 | A | AT | 124 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(121): Show |
135 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.302+159dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 3/7 | chr2 | 69423422 | |||||||
chr2:69423741 | G | A | 1 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0210 | 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 | 3 | a0002c0002t0001g0016 a0002c0002t0001g0259 a0002c0002t0001g0308 |
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 | a0001c0001t0001g0172 | 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 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0001g0338 others(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 | 33 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0074 others(30): 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 | a0001c0001t0001g0067 a0001c0001t0001g0115 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0245 a0002c0002t0001g0247 others(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 | 34 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(31): 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 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0086 others(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 | 36 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(33): 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 | 30 | a0001c0001t0001g0008 a0001c0001t0001g0074 a0001c0001t0001g0117 others(27): 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 | a0001c0001t0001g0222 | 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 | a0003c0004t0001g0151 a0003c0004t0001g0152 a0003c0004t0001g0153 others(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 | a0002c0002t0001g0247 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0114 others(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 | 33 | a0002c0002t0001g0001 a0002c0002t0001g0014 a0002c0002t0001g0017 others(30): Show |
38 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(35): 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 | a0001c0001t0001g0329 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0334 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0336 |
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 | a0001c0001t0001g0335 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0337 | 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 | 63 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0023 others(60): 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0193 others(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 | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0334 a0003c0004t0001g0150 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0225 | 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 | 183 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(180): Show |
196 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.167-1162dupA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69424878 | |||||||
chr2:69424878 | C | CTT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0081 others(31): 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0226 | 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 | a0002c0002t0001g0299 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.167-1610G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425327 | |||||||
chr2:69425358 | AT | A | 228 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
242 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.167-1642delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69425358 | |||||||
chr2:69425505 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0003c0004t0001g0150 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0148 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0334 | 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 | a0002c0002t0001g0300 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0002c0002t0001g0250 a0002c0002t0001g0301 a0002c0002t0001g0302 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 173 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(170): Show |
184 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(181): 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.167-3532C>G | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69427249 | |||||||
chr2:69427254 | A | G | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 46 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(43): 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0001c0001t0001g0230 | 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 | 19 | a0001c0001t0001g0008 a0001c0001t0001g0117 a0001c0001t0001g0118 others(16): 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 | a0001c0001t0001g0148 a0001c0001t0001g0334 a0001c0001t0001g0335 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0334 a0001c0001t0001g0335 others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0334 a0001c0001t0001g0335 others(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 | a0001c0001t0001g0232 | 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(122): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): 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 | a0002c0002t0001g0254 | 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 | a0003c0004t0001g0150 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0057 |
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 | a0002c0002t0001g0253 a0002c0002t0001g0309 a0002c0002t0001g0310 others(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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(32): 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0083 | 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0002c0002t0001g0314 a0002c0002t0001g0315 a0002c0002t0001g0316 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0075 |
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 | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
241 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.166+1684delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 2/7 | chr2 | 69430217 | |||||||
chr2:69430352 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0148 | 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0057 |
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 | a0002c0002t0001g0318 | 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 | a0002c0002t0001g0318 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0233 a0001c0001t0001g0234 others(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 | 20 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0117 others(17): 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0002c0002t0001g0322 | 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 | a0002c0002t0001g0317 | 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 | a0001c0001t0001g0148 | 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 | a0002c0002t0001g0253 | 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 | 128 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(125): Show |
140 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(137): 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): 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 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): 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 | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): 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 | a0001c0001t0001g0063 a0001c0001t0002g0342 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(160): Show |
175 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.63-1146dupT | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433150 | |||||||
chr2:69433150 | C | CAA | 16 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0136 | 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 | a0003c0004t0001g0150 a0003c0004t0001g0151 a0003c0004t0001g0152 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(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 | a0002c0002t0001g0322 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0081 others(32): 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 | 151 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0023 others(148): Show |
163 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.63-1936delA | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69433940 | |||||||
chr2:69433940 | GTT | G | 41 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0063 others(38): 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 | a0001c0001t0001g0063 a0001c0001t0002g0342 |
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 | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.63-2144G>A | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69434149 | |||||||
chr2:69434150 | T | C | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
246 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(243): 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 | a0001c0001t0001g0114 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
250 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(247): 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 | a0001c0001t0001g0148 a0001c0001t0001g0334 a0001c0001t0001g0335 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0059 | 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 | 30 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0073 others(27): 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
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 | 28 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0074 others(25): 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 | a0001c0001t0001g0243 | 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 | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0071 others(42): 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0246 | 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 | 92 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0002g0342 others(89): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(99): 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0332 | 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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0063 a0001c0001t0002g0342 |
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 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0002c0002t0001g0338 a0002c0002t0001g0339 |
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 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.62+9C>T | NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1/7 | chr2 | 69437352 |