Item | Value |
---|---|
geneid | 2733 |
ensemblid | ENSG00000119392.16 |
hgncid | 4315 |
symbol | GLE1 |
name | GLE1 RNA export mediator |
refseq_nuc | NM_001003722.2 |
refseq_prot | NP_001003722.1 |
ensembl_nuc | ENST00000309971.9 |
ensembl_prot | ENSP00000308622.5 |
mane_status | MANE Select |
chr | chr9 |
start | 128504719 |
end | 128542288 |
strand | + |
ver | v1.2 |
region | chr9:128504719-128542288 |
region5000 | chr9:128499719-128547288 |
regionname0 | GLE1_chr9_128504719_128542288 |
regionname5000 | GLE1_chr9_128499719_128547288 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 698 | 192 | 49 | 37 | 77 | 6 | 21 | 61 | GLE1_chr9_128499719_128547288 | GLE1 | MPSEG others(693): Show |
chr9 | 128499719 | 128547288 |
a0002 | 0/0 | 698 | 165 | 32 | 21 | 93 | 4 | 15 | 75 | GLE1_chr9_128499719_128547288 | GLE1 | MPSEG others(693): Show |
chr9 | 128499719 | 128547288 |
a0003 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | MPSEG others(693): Show |
chr9 | 128499719 | 128547288 |
a0004 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | MPSEG others(693): Show |
chr9 | 128499719 | 128547288 |
a0005 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | MPSEG others(693): Show |
chr9 | 128499719 | 128547288 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2094 | 191 | 49 | 37 | 76 | 6 | 21 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0001c0006 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0002c0002 | 0/0 | 2094 | 162 | 32 | 21 | 90 | 4 | 15 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0002c0003 | 0/0 | 2094 | 2 | 0 | 0 | 2 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0002c0007 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0003c0008 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0004c0005 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 | ||
a0005c0004 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | ATGCC others(2089): Show |
chr9 | 128499719 | 128547288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3302 | 183 | 48 | 34 | 74 | 4 | 21 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0001t0004 | 0/0 | 3302 | 4 | 0 | 3 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0001t0005 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0001t0006 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0001t0007 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0001t0008 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0001c0006t0001 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0002c0002t0001 | 0/0 | 3302 | 20 | 17 | 3 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0002c0002t0002 | 0/0 | 3302 | 114 | 15 | 15 | 66 | 4 | 14 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0002c0002t0003 | 0/0 | 3302 | 28 | 0 | 3 | 24 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0002c0003t0002 | 0/0 | 3302 | 2 | 0 | 0 | 2 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0002c0007t0002 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0003c0008t0001 | 0/0 | 3302 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0004c0005t0001 | 0/0 | 3302 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
a0005c0004t0001 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | AGAAG others(3297): Show |
chr9 | 128499719 | 128547288 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0002c0007t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0003c0008t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0004c0005t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
a0005c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0002 | g0230 | EUR | FIN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0202 | EUR | FIN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00609 | hp1 | a0002 | c0002 | t0003 | g0285 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0051 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | CHS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0234 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01099 | hp2 | a0002 | c0002 | t0003 | g0297 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0336 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0253 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0335 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01261 | hp2 | a0003 | c0008 | t0001 | g0302 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0277 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0319 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0172 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0227 | EUR | IBS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0338 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01975 | hp1 | a0002 | c0002 | t0003 | g0296 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0330 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02004 | hp2 | a0004 | c0005 | t0001 | g0020 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0304 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0292 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02040 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02129 | hp2 | a0002 | c0003 | t0002 | g0303 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | CDX | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0317 | EAS | CDX | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0340 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0341 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0217 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0170 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0282 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0228 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0229 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0321 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0211 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0210 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0216 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0206 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0312 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0327 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0222 | SAS | BEB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0175 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | STU | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0288 | EAS | CHB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | CHB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18906 | hp1 | a0005 | c0004 | t0001 | g0140 | AFR | YRI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | YRI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0280 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0290 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0276 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18962 | hp1 | a0002 | c0002 | t0003 | g0299 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18975 | hp1 | a0002 | c0002 | t0003 | g0278 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18984 | hp1 | a0002 | c0002 | t0003 | g0300 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0332 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18990 | hp1 | a0002 | c0002 | t0003 | g0294 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0279 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18998 | hp1 | a0002 | c0007 | t0002 | g0187 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0289 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19012 | hp1 | a0002 | c0002 | t0003 | g0286 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0219 | AFR | LWK | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19055 | hp1 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19055 | hp2 | a0002 | c0002 | t0003 | g0281 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0283 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19059 | hp1 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0275 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0295 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19068 | hp2 | a0002 | c0002 | t0003 | g0298 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0284 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19081 | hp1 | a0002 | c0002 | t0003 | g0291 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0318 | AFR | ASW | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0023 | EUR | TSI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0226 | EUR | TSI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | TSI | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0329 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | USA | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0108 | REF | REF | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0257 | REF | REF | GLE1_chr9_128499719_128547288 | GLE1 | chr9 | 128499719 | 128547288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128508942 | G | A | 1 | a0005 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.166G>A | p.Val56Ile | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/16 | 253/3302 | 166/2097 | 56/698 | chr9 | 128508942 | |||
chr9:128523595 | C | G | 1 | a0003 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.646C>G | p.Leu216Val | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/16 | 733/3302 | 646/2097 | 216/698 | chr9 | 128523595 | |||
chr9:128523676 | A | G | 1 | a0002 | 165 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
missense_variant | MODERATE | c.727A>G | p.Ile243Val | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/16 | 814/3302 | 727/2097 | 243/698 | chr9 | 128523676 | |||
chr9:128525294 | G | A | 1 | a0004 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.1000G>A | p.Glu334Lys | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/16 | 1087/3302 | 1000/2097 | 334/698 | chr9 | 128525294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128522679 | G | A | 1 | a0002c0003 | 2 | HG02027.hp1 HG02129.hp2 |
synonymous_variant | LOW | c.444G>A | p.Arg148Arg | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 4/16 | 531/3302 | 444/2097 | 148/698 | chr9 | 128522679 | |||
chr9:128523771 | C | T | 1 | a0002c0007 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.822C>T | p.Val274Val | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/16 | 909/3302 | 822/2097 | 274/698 | chr9 | 128523771 | |||
chr9:128533946 | T | C | 1 | a0001c0006 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.1641T>C | p.Tyr547Tyr | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/16 | 1728/3302 | 1641/2097 | 547/698 | chr9 | 128533946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128541243 | G | A | 3 | a0002c0002t0002 a0002c0003t0002 a0002c0007t0002 |
117 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 73 | chr9 | 128541243 | ||||||
chr9:128541351 | C | A | 1 | a0001c0001t0004 | 4 | HG01256.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*181C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 181 | chr9 | 128541351 | ||||||
chr9:128541461 | C | G | 1 | a0001c0001t0008 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*291C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 291 | chr9 | 128541461 | ||||||
chr9:128541519 | G | A | 1 | a0001c0001t0005 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*349G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 349 | chr9 | 128541519 | ||||||
chr9:128541557 | C | G | 1 | a0002c0002t0003 | 28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*387C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 387 | chr9 | 128541557 | ||||||
chr9:128542077 | G | C | 1 | a0001c0001t0004 | 4 | HG01256.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*907G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 907 | chr9 | 128542077 | ||||||
chr9:128542175 | T | C | 2 | a0001c0001t0006 a0002c0002t0003 |
29 | HG00609.hp1 HG00673.hp1 HG01099.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1005T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 1005 | chr9 | 128542175 | ||||||
chr9:128542261 | T | C | 1 | a0001c0001t0007 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1091T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 16/16 | 1091 | chr9 | 128542261 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:128504933 | C | G | 36 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 others(33): Show |
36 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+29C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128504933 | |||||||
chr9:128504987 | C | G | 4 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0001g0030 others(1): Show |
4 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+83C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128504987 | |||||||
chr9:128505147 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+243C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505147 | |||||||
chr9:128505245 | A | G | 2 | a0002c0003t0002g0303 a0002c0003t0002g0304 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.99+341A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505245 | |||||||
chr9:128505343 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.99+439G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505343 | |||||||
chr9:128505643 | T | C | 1 | a0002c0002t0003g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.99+739T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505643 | |||||||
chr9:128505671 | A | G | 2 | a0001c0001t0001g0301 a0003c0008t0001g0302 |
2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.99+767A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505671 | |||||||
chr9:128505839 | T | G | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+935T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505839 | |||||||
chr9:128505865 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+961G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505865 | |||||||
chr9:128505917 | C | T | 9 | a0002c0002t0003g0292 a0002c0002t0003g0293 a0002c0002t0003g0294 others(6): Show |
9 | HG01099.hp2 HG01975.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+1013C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505917 | |||||||
chr9:128505937 | G | T | 13 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0331 others(10): Show |
13 | HG01106.hp2 HG01123.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+1033G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505937 | |||||||
chr9:128505991 | A | G | 27 | a0002c0002t0003g0015 a0002c0002t0003g0275 a0002c0002t0003g0276 others(24): Show |
27 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.99+1087A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128505991 | |||||||
chr9:128506308 | G | A | 1 | a0002c0002t0002g0329 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+1404G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506308 | |||||||
chr9:128506395 | A | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0263 a0001c0001t0001g0264 others(10): Show |
14 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+1491A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506395 | |||||||
chr9:128506422 | T | G | 1 | a0002c0002t0002g0019 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.99+1518T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506422 | |||||||
chr9:128506527 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.99+1623C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506527 | |||||||
chr9:128506763 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.99+1859C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506763 | |||||||
chr9:128506956 | T | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.100-1920T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128506956 | |||||||
chr9:128507134 | G | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-1742G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507134 | |||||||
chr9:128507210 | T | C | 1 | a0004c0005t0001g0020 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.100-1666T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507210 | |||||||
chr9:128507455 | G | A | 1 | a0002c0002t0001g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100-1421G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507455 | |||||||
chr9:128507534 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-1342T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507534 | |||||||
chr9:128507585 | CA | C | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG01256.hp1 HG01256.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-1272delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr9 | 128507585 | ||||||
chr9:128507604 | A | G | 1 | a0002c0002t0001g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-1272A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507604 | |||||||
chr9:128507727 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18946.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.100-1149A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507727 | |||||||
chr9:128507773 | A | T | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-1103A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507773 | |||||||
chr9:128507977 | C | G | 116 | a0001c0001t0001g0171 a0002c0002t0001g0012 a0002c0002t0001g0169 others(113): Show |
121 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.100-899C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128507977 | |||||||
chr9:128508010 | G | A | 1 | a0001c0001t0008g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.100-866G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508010 | |||||||
chr9:128508026 | C | T | 1 | a0002c0002t0002g0235 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.100-850C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508026 | |||||||
chr9:128508090 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.100-786G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508090 | |||||||
chr9:128508112 | G | T | 1 | a0002c0002t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.100-764G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508112 | |||||||
chr9:128508114 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-762A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508114 | |||||||
chr9:128508166 | G | A | 1 | a0002c0002t0002g0306 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.100-710G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508166 | |||||||
chr9:128508180 | C | CA | 151 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(148): Show |
157 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.100-678dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr9 | 128508180 | ||||||
chr9:128508180 | C | CAA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0263 a0001c0001t0001g0264 others(16): Show |
20 | HG01109.hp1 HG01192.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-679_100-678dup others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr9 | 128508180 | ||||||
chr9:128508180 | CA | C | 7 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG01256.hp2 HG01257.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-678delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr9 | 128508180 | ||||||
chr9:128508201 | C | T | 129 | a0002c0002t0001g0012 a0002c0002t0001g0021 a0002c0002t0001g0024 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.100-675C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508201 | |||||||
chr9:128508297 | G | T | 36 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 others(33): Show |
36 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100-579G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508297 | |||||||
chr9:128508562 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA18983.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.100-314T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 1/15 | chr9 | 128508562 | |||||||
chr9:128509335 | AT | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
15 | HG00558.hp1 HG00558.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+251delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128509335 | ||||||
chr9:128509492 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.321+395C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509492 | |||||||
chr9:128509651 | C | CA | 109 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0045 others(106): Show |
115 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.321+570dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128509651 | ||||||
chr9:128509651 | C | CAA | 42 | a0001c0001t0001g0013 a0001c0001t0001g0263 a0001c0001t0001g0264 others(39): Show |
43 | HG00621.hp2 HG00673.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.321+569_321+570dup others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128509651 | ||||||
chr9:128509703 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(1): Show |
4 | HG02129.hp1 NA19000.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+606A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509703 | |||||||
chr9:128509704 | A | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(15): Show |
19 | HG02074.hp1 HG02080.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.321+607A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509704 | |||||||
chr9:128509734 | G | A | 1 | a0001c0001t0006g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.321+637G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509734 | |||||||
chr9:128509850 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.321+753T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509850 | |||||||
chr9:128509856 | C | T | 27 | a0002c0002t0003g0015 a0002c0002t0003g0275 a0002c0002t0003g0276 others(24): Show |
27 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+759C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509856 | |||||||
chr9:128509958 | CA | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
158 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.321+869delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128509958 | ||||||
chr9:128509965 | A | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(9): Show |
12 | HG01358.hp1 HG01884.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.321+868A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128509965 | |||||||
chr9:128510094 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.321+997G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510094 | |||||||
chr9:128510107 | G | T | 1 | a0002c0002t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.321+1010G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510107 | |||||||
chr9:128510154 | C | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0167 a0002c0002t0002g0172 others(37): Show |
43 | HG00280.hp2 HG01433.hp2 HG02027.hp1 others(40): Show |
intron_variant | MODIFIER | c.321+1057C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510154 | |||||||
chr9:128510234 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0056 others(6): Show |
9 | HG00280.hp1 HG02886.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+1149dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128510234 | ||||||
chr9:128510251 | C | T | 8 | a0002c0002t0002g0224 a0002c0002t0002g0225 a0002c0002t0002g0226 others(5): Show |
8 | HG00280.hp1 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.321+1154C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510251 | |||||||
chr9:128510252 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.321+1155G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510252 | |||||||
chr9:128510298 | A | G | 3 | a0002c0002t0002g0184 a0002c0002t0002g0223 a0002c0002t0002g0234 |
3 | HG01069.hp1 HG01167.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.321+1201A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510298 | |||||||
chr9:128510311 | T | C | 175 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0055 others(172): Show |
181 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.321+1214T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510311 | |||||||
chr9:128510322 | G | A | 1 | a0002c0002t0003g0293 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.321+1225G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510322 | |||||||
chr9:128510526 | C | CT | 26 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(23): Show |
26 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.321+1449dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128510526 | ||||||
chr9:128510526 | CT | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.321+1449delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128510526 | ||||||
chr9:128510630 | G | A | 15 | a0002c0002t0002g0019 a0002c0002t0002g0168 a0002c0002t0002g0178 others(12): Show |
15 | HG00673.hp2 HG02071.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+1533G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510630 | |||||||
chr9:128510678 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.321+1581G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510678 | |||||||
chr9:128510727 | C | T | 27 | a0002c0002t0003g0015 a0002c0002t0003g0275 a0002c0002t0003g0276 others(24): Show |
27 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+1630C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510727 | |||||||
chr9:128510808 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+1711C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510808 | |||||||
chr9:128510830 | G | GT | 35 | a0001c0001t0001g0121 a0001c0001t0001g0271 a0002c0002t0001g0005 others(32): Show |
36 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.321+1749dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128510830 | ||||||
chr9:128510830 | GT | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0122 others(12): Show |
15 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+1749delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128510830 | ||||||
chr9:128510902 | T | A | 1 | a0002c0002t0002g0327 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.321+1805T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128510902 | |||||||
chr9:128511102 | G | A | 1 | a0002c0002t0002g0329 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.321+2005G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511102 | |||||||
chr9:128511123 | G | A | 1 | a0002c0002t0002g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.321+2026G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511123 | |||||||
chr9:128511169 | A | G | 1 | a0002c0002t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.321+2072A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511169 | |||||||
chr9:128511183 | A | G | 1 | a0002c0002t0003g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.321+2086A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511183 | |||||||
chr9:128511232 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.321+2135A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511232 | |||||||
chr9:128511297 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.321+2200G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511297 | |||||||
chr9:128511327 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.321+2230G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511327 | |||||||
chr9:128511345 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.321+2248T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511345 | |||||||
chr9:128511432 | G | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+2335G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511432 | |||||||
chr9:128511574 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.321+2477C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511574 | |||||||
chr9:128511705 | CA | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0263 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+2623delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128511705 | ||||||
chr9:128511744 | A | G | 159 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(156): Show |
165 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.321+2647A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511744 | |||||||
chr9:128511993 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.321+2896G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128511993 | |||||||
chr9:128512514 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0062 |
2 | HG01175.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.322-3015T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128512514 | |||||||
chr9:128512590 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.322-2939G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128512590 | |||||||
chr9:128512793 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0218 |
3 | HG02109.hp1 HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.322-2736G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128512793 | |||||||
chr9:128513068 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.322-2461C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513068 | |||||||
chr9:128513145 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.322-2384C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513145 | |||||||
chr9:128513188 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0264 a0001c0001t0001g0272 |
4 | HG02559.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-2341T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513188 | |||||||
chr9:128513221 | A | G | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.322-2308A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513221 | |||||||
chr9:128513409 | T | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.322-2120T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513409 | |||||||
chr9:128513410 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.322-2119C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513410 | |||||||
chr9:128513560 | A | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.322-1969A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513560 | |||||||
chr9:128513574 | A | G | 129 | a0002c0002t0001g0012 a0002c0002t0001g0021 a0002c0002t0001g0024 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.322-1955A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513574 | |||||||
chr9:128513708 | C | CA | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0135 others(5): Show |
8 | HG00735.hp1 HG00735.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.322-1807dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128513708 | ||||||
chr9:128513745 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0123 |
3 | HG01168.hp2 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.322-1784G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513745 | |||||||
chr9:128513783 | A | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.322-1746A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513783 | |||||||
chr9:128513787 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0273 a0001c0001t0005g0269 |
3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.322-1742C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513787 | |||||||
chr9:128513848 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.322-1681C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128513848 | |||||||
chr9:128514011 | C | T | 36 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 others(33): Show |
36 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.322-1518C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514011 | |||||||
chr9:128514017 | CA | C | 142 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0002c0002t0001g0012 others(139): Show |
147 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.322-1497delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514017 | ||||||
chr9:128514026 | AAAAAAAG | A | 13 | a0002c0002t0002g0019 a0002c0002t0002g0168 a0002c0002t0002g0178 others(10): Show |
13 | HG00673.hp2 HG02071.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-1497_322-1491d others(9): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514026 | ||||||
chr9:128514029 | A | G | 1 | a0002c0002t0002g0326 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.322-1500A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514029 | |||||||
chr9:128514086 | G | A | 2 | a0002c0002t0002g0314 a0002c0002t0002g0315 |
2 | NA18970.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.322-1443G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514086 | |||||||
chr9:128514255 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.322-1274A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514255 | |||||||
chr9:128514292 | T | G | 4 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0001g0030 others(1): Show |
4 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-1237T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514292 | |||||||
chr9:128514338 | C | CA | 28 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0038 others(25): Show |
28 | HG00609.hp2 HG00621.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.322-1170dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514338 | ||||||
chr9:128514338 | CA | C | 148 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(145): Show |
154 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.322-1170delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514338 | ||||||
chr9:128514445 | C | CT | 30 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0118 others(27): Show |
30 | HG01109.hp2 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.322-1065dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514445 | ||||||
chr9:128514445 | CT | C | 26 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(23): Show |
26 | HG00673.hp2 HG02071.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.322-1065delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128514445 | ||||||
chr9:128514717 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
172 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.322-812G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514717 | |||||||
chr9:128514786 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0123 |
3 | HG01168.hp2 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.322-743A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514786 | |||||||
chr9:128514787 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.322-742C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128514787 | |||||||
chr9:128515009 | C | T | 2 | a0002c0002t0001g0012 a0002c0002t0001g0169 |
3 | HG02965.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.322-520C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128515009 | |||||||
chr9:128515114 | C | T | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.322-415C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128515114 | |||||||
chr9:128515331 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.322-198T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | chr9 | 128515331 | |||||||
chr9:128515490 | CTTATTTT | C | 159 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(156): Show |
165 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.322-35_322-29delTT others(5): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr9 | 128515490 | ||||||
chr9:128515744 | C | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432+105C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515744 | |||||||
chr9:128515750 | G | A | 1 | a0002c0002t0002g0234 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.432+111G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515750 | |||||||
chr9:128515760 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+121G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515760 | |||||||
chr9:128515774 | A | G | 1 | a0002c0002t0002g0327 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.432+135A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515774 | |||||||
chr9:128515786 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.432+147T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515786 | |||||||
chr9:128515801 | CAA | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432+163_432+164del others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515801 | |||||||
chr9:128515849 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+210G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128515849 | |||||||
chr9:128515952 | C | CT | 173 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0053 others(170): Show |
179 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.432+328dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128515952 | ||||||
chr9:128516040 | T | G | 1 | a0002c0002t0002g0011 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.432+401T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516040 | |||||||
chr9:128516067 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.432+428C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516067 | |||||||
chr9:128516325 | T | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432+686T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516325 | |||||||
chr9:128516476 | C | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432+837C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516476 | |||||||
chr9:128516520 | C | T | 1 | a0002c0002t0002g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.432+881C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516520 | |||||||
chr9:128516521 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+882G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516521 | |||||||
chr9:128516534 | C | T | 3 | a0002c0002t0001g0240 a0002c0002t0002g0183 a0002c0002t0002g0220 |
3 | HG02559.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.432+895C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516534 | |||||||
chr9:128516619 | TG | T | 14 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0073 others(11): Show |
14 | HG00423.hp2 HG00558.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+981delG | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516619 | |||||||
chr9:128516827 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432+1188T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516827 | |||||||
chr9:128516972 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+1333G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128516972 | |||||||
chr9:128517018 | G | A | 3 | a0001c0001t0001g0263 a0002c0002t0001g0005 a0002c0002t0001g0245 |
4 | HG02055.hp1 HG02109.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1379G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517018 | |||||||
chr9:128517215 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+1576G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517215 | |||||||
chr9:128517229 | G | A | 17 | a0002c0002t0002g0002 a0002c0002t0002g0173 a0002c0002t0002g0174 others(14): Show |
20 | HG02071.hp1 HG02074.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.432+1590G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517229 | |||||||
chr9:128517307 | A | T | 2 | a0002c0002t0001g0012 a0002c0002t0001g0169 |
3 | HG02965.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.432+1668A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517307 | |||||||
chr9:128517342 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+1703G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517342 | |||||||
chr9:128517446 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+1807G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517446 | |||||||
chr9:128517573 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.432+1934A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517573 | |||||||
chr9:128517585 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.432+1946T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517585 | |||||||
chr9:128517733 | A | G | 4 | a0002c0002t0002g0313 a0002c0002t0002g0323 a0002c0002t0002g0324 others(1): Show |
4 | HG00423.hp1 NA18956.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+2094A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517733 | |||||||
chr9:128517743 | C | A | 2 | a0002c0002t0002g0224 a0002c0002t0002g0225 |
2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.432+2104C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517743 | |||||||
chr9:128517745 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.432+2106C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128517745 | |||||||
chr9:128518145 | G | A | 1 | a0005c0004t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.432+2506G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518145 | |||||||
chr9:128518156 | A | AT | 12 | a0001c0001t0001g0072 a0001c0001t0001g0137 a0001c0001t0001g0158 others(9): Show |
12 | HG01074.hp1 HG01109.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.432+2530dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128518156 | ||||||
chr9:128518302 | T | C | 4 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0001g0030 others(1): Show |
4 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+2663T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518302 | |||||||
chr9:128518412 | T | C | 3 | a0002c0002t0002g0184 a0002c0002t0002g0223 a0002c0002t0002g0234 |
3 | HG01069.hp1 HG01167.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.432+2773T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518412 | |||||||
chr9:128518516 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.432+2877G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518516 | |||||||
chr9:128518652 | G | A | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+3013G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518652 | |||||||
chr9:128518799 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0137 a0001c0001t0001g0139 |
3 | HG00735.hp1 HG01358.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.432+3160C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518799 | |||||||
chr9:128518862 | C | CA | 9 | a0001c0001t0001g0055 a0001c0001t0001g0073 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp1 HG03209.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.432+3239dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128518862 | ||||||
chr9:128518874 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0056 others(3): Show |
6 | HG02886.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+3235A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518874 | |||||||
chr9:128518878 | A | G | 1 | a0002c0002t0002g0221 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.432+3239A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128518878 | |||||||
chr9:128519028 | A | G | 2 | a0001c0001t0001g0059 a0002c0002t0003g0288 |
2 | NA18612.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.432+3389A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519028 | |||||||
chr9:128519153 | C | T | 1 | a0002c0002t0002g0337 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.432+3514C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519153 | |||||||
chr9:128519300 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0264 a0001c0001t0001g0272 |
4 | HG02559.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3368C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519300 | |||||||
chr9:128519361 | C | T | 2 | a0001c0001t0001g0110 a0002c0002t0002g0336 |
2 | HG01106.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.433-3307C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519361 | |||||||
chr9:128519362 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3306G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519362 | |||||||
chr9:128519409 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.433-3259G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519409 | |||||||
chr9:128519410 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.433-3258C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519410 | |||||||
chr9:128519644 | CTGGTCCT others(1): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0264 a0001c0001t0001g0272 |
4 | HG02559.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3005_433-2998d others(10): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128519644 | ||||||
chr9:128519678 | G | A | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-2990G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519678 | |||||||
chr9:128519684 | G | A | 1 | a0002c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.433-2984G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519684 | |||||||
chr9:128519685 | C | T | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.433-2983C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519685 | |||||||
chr9:128519714 | G | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.433-2954G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519714 | |||||||
chr9:128519758 | G | A | 6 | a0002c0002t0002g0185 a0002c0002t0002g0196 a0002c0002t0002g0197 others(3): Show |
6 | NA18945.hp2 NA18968.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-2910G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519758 | |||||||
chr9:128519854 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0154 a0002c0002t0003g0287 others(1): Show |
4 | HG02040.hp2 NA18987.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-2814C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519854 | |||||||
chr9:128519981 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0074 |
3 | HG00558.hp2 NA18993.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.433-2687G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128519981 | |||||||
chr9:128520023 | G | A | 5 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0002c0002t0002g0184 others(2): Show |
5 | HG01069.hp1 HG01167.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-2645G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520023 | |||||||
chr9:128520110 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-2558C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520110 | |||||||
chr9:128520111 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.433-2557G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520111 | |||||||
chr9:128520113 | G | T | 1 | a0001c0001t0001g0027 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.433-2555G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520113 | |||||||
chr9:128520120 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.433-2548C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520120 | |||||||
chr9:128520308 | A | G | 1 | a0002c0002t0002g0204 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.433-2360A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520308 | |||||||
chr9:128520326 | GTGTGTAT others(1): Show |
G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0141 others(5): Show |
9 | HG02055.hp1 HG02109.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-2324_433-2317d others(10): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520326 | ||||||
chr9:128520336 | G | GTGTATAT others(33): Show |
1 | a0001c0001t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-2325_433-2324i others(42): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520336 | ||||||
chr9:128520336 | G | GTGTATAT others(33): Show |
5 | a0001c0001t0001g0065 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-2290_433-2251d others(42): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520336 | ||||||
chr9:128520336 | GTGTATAT others(33): Show |
G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA18983.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.433-2290_433-2251d others(42): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520336 | ||||||
chr9:128520344 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2324G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520344 | |||||||
chr9:128520348 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.433-2320A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520348 | |||||||
chr9:128520350 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2318A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520350 | |||||||
chr9:128520352 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2316A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520352 | |||||||
chr9:128520358 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2310G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520358 | |||||||
chr9:128520358 | GTGTGTAT others(3): Show |
G | 1 | a0002c0002t0002g0333 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.433-2306_433-2297d others(12): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520358 | ||||||
chr9:128520360 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2308G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520360 | |||||||
chr9:128520360 | GTGTATAT others(1): Show |
G | 35 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 others(32): Show |
35 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.433-2292_433-2285d others(10): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520360 | ||||||
chr9:128520376 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-2292A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520376 | |||||||
chr9:128520440 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.433-2228A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520440 | |||||||
chr9:128520444 | A | G | 1 | a0002c0002t0002g0235 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.433-2224A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520444 | |||||||
chr9:128520449 | TA | T | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.433-2213delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520449 | ||||||
chr9:128520451 | A | T | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-2217A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520451 | |||||||
chr9:128520603 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.433-2065C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520603 | |||||||
chr9:128520692 | C | CGT | 7 | a0002c0002t0001g0005 a0002c0002t0001g0024 a0002c0002t0001g0028 others(4): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.433-1961_433-1960d others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520692 | ||||||
chr9:128520757 | A | AT | 10 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0057 others(7): Show |
10 | HG01069.hp1 HG01167.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-1898dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520757 | ||||||
chr9:128520757 | AT | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0078 others(6): Show |
9 | HG01069.hp2 HG01361.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-1898delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128520757 | ||||||
chr9:128520882 | C | A | 129 | a0002c0002t0001g0012 a0002c0002t0001g0021 a0002c0002t0001g0024 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.433-1786C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520882 | |||||||
chr9:128520951 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-1717C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128520951 | |||||||
chr9:128521023 | A | C | 3 | a0002c0002t0002g0180 a0002c0002t0002g0214 a0002c0002t0002g0215 |
3 | HG02071.hp2 NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.433-1645A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521023 | |||||||
chr9:128521249 | A | T | 1 | a0002c0002t0002g0322 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.433-1419A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521249 | |||||||
chr9:128521400 | A | T | 1 | a0002c0002t0002g0017 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433-1268A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521400 | |||||||
chr9:128521502 | C | G | 6 | a0002c0002t0001g0012 a0002c0002t0001g0024 a0002c0002t0001g0028 others(3): Show |
7 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-1166C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521502 | |||||||
chr9:128521907 | G | A | 4 | a0002c0002t0002g0333 a0002c0002t0002g0334 a0002c0002t0002g0337 others(1): Show |
4 | NA18953.hp1 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-761G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521907 | |||||||
chr9:128521924 | A | G | 4 | a0002c0002t0003g0275 a0002c0002t0003g0279 a0002c0002t0003g0286 others(1): Show |
4 | NA18993.hp1 NA19012.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-744A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128521924 | |||||||
chr9:128522047 | A | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.433-621A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522047 | |||||||
chr9:128522178 | A | G | 4 | a0002c0002t0002g0203 a0002c0002t0002g0204 a0002c0002t0002g0254 others(1): Show |
4 | NA18998.hp1 NA19060.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-490A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522178 | |||||||
chr9:128522315 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.433-353C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522315 | |||||||
chr9:128522382 | C | G | 1 | a0002c0002t0002g0207 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.433-286C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522382 | |||||||
chr9:128522383 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.433-285G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522383 | |||||||
chr9:128522558 | C | T | 1 | a0002c0002t0002g0306 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.433-110C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522558 | |||||||
chr9:128522635 | T | TA | 10 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0001g0256 others(7): Show |
10 | HG02027.hp2 HG02486.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-10dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128522635 | ||||||
chr9:128522635 | TA | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
279 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.433-10delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128522635 | ||||||
chr9:128522635 | TAA | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0135 others(10): Show |
13 | HG02451.hp2 HG02970.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-11_433-10delAA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr9 | 128522635 | ||||||
chr9:128522653 | A | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG02717.hp1 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.433-15A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 3/15 | chr9 | 128522653 | |||||||
chr9:128522981 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.581+165G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 4/15 | chr9 | 128522981 | |||||||
chr9:128523144 | G | A | 2 | a0002c0002t0002g0183 a0002c0002t0002g0220 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.582-136G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 4/15 | chr9 | 128523144 | |||||||
chr9:128523145 | C | A | 2 | a0002c0002t0002g0183 a0002c0002t0002g0220 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.582-135C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 4/15 | chr9 | 128523145 | |||||||
chr9:128523516 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.643-76A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 5/15 | chr9 | 128523516 | |||||||
chr9:128523545 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.643-47A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 5/15 | chr9 | 128523545 | |||||||
chr9:128524072 | C | CT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0264 a0001c0001t0001g0265 others(6): Show |
10 | HG02559.hp2 HG02809.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.897+251dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524072 | CT | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(16): Show |
20 | HG01109.hp2 HG01358.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.897+251delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524072 | CTT | C | 42 | a0001c0001t0001g0055 a0002c0002t0001g0028 a0002c0002t0001g0029 others(39): Show |
42 | HG00609.hp1 HG01099.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.897+250_897+251del others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524072 | CTTT | C | 102 | a0002c0002t0001g0012 a0002c0002t0001g0024 a0002c0002t0001g0031 others(99): Show |
107 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.897+249_897+251del others(3): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524072 | CTTTT | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(12): Show |
17 | HG01106.hp1 HG01175.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.897+248_897+251del others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524072 | CTTTTT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(127): Show |
139 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.897+247_897+251del others(5): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524072 | ||||||
chr9:128524540 | C | CT | 45 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0065 others(42): Show |
45 | HG00423.hp1 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.898-623dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524540 | ||||||
chr9:128524540 | C | CTT | 15 | a0002c0002t0002g0167 a0002c0002t0003g0015 a0002c0002t0003g0276 others(12): Show |
15 | HG00609.hp1 HG01361.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.898-624_898-623dup others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524540 | ||||||
chr9:128524540 | C | CTTTT | 8 | a0002c0002t0003g0279 a0002c0002t0003g0284 a0002c0002t0003g0286 others(5): Show |
8 | HG01099.hp2 HG01975.hp1 NA18993.hp1 others(5): Show |
intron_variant | MODIFIER | c.898-626_898-623dup others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524540 | ||||||
chr9:128524540 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
123 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.898-623delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr9 | 128524540 | ||||||
chr9:128524582 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.898-610C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128524582 | |||||||
chr9:128524638 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0056 others(5): Show |
8 | HG02886.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-554G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128524638 | |||||||
chr9:128524717 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.898-475C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128524717 | |||||||
chr9:128524731 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.898-461A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128524731 | |||||||
chr9:128524839 | C | G | 113 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0016 others(110): Show |
117 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.898-353C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128524839 | |||||||
chr9:128525073 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
157 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.898-119C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 6/15 | chr9 | 128525073 | |||||||
chr9:128525677 | C | T | 129 | a0002c0002t0001g0012 a0002c0002t0001g0021 a0002c0002t0001g0024 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1129+254C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128525677 | |||||||
chr9:128525746 | G | A | 6 | a0002c0002t0001g0012 a0002c0002t0001g0024 a0002c0002t0001g0028 others(3): Show |
7 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129+323G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128525746 | |||||||
chr9:128526000 | TTTGTTGT others(5): Show |
T | 1 | a0002c0002t0002g0220 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129+592_1129+603d others(14): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr9 | 128526000 | ||||||
chr9:128526027 | T | G | 1 | a0005c0004t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1129+604T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526027 | |||||||
chr9:128526083 | G | A | 1 | a0002c0002t0002g0011 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1129+660G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526083 | |||||||
chr9:128526146 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1129+723C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526146 | |||||||
chr9:128526162 | C | T | 131 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(128): Show |
137 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1129+739C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526162 | |||||||
chr9:128526190 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1129+767T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526190 | |||||||
chr9:128526349 | T | G | 3 | a0002c0002t0002g0180 a0002c0002t0002g0214 a0002c0002t0002g0215 |
3 | HG02071.hp2 NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1130-830T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526349 | |||||||
chr9:128526364 | T | G | 1 | a0002c0002t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1130-815T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526364 | |||||||
chr9:128526365 | G | T | 1 | a0002c0002t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1130-814G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526365 | |||||||
chr9:128526442 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1130-737C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526442 | |||||||
chr9:128526657 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1130-522C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526657 | |||||||
chr9:128526658 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1130-521G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526658 | |||||||
chr9:128526819 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0132 a0001c0001t0001g0134 |
3 | HG01884.hp1 HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1130-360G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526819 | |||||||
chr9:128526882 | C | A | 19 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0055 others(16): Show |
19 | HG00735.hp1 HG01358.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1130-297C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128526882 | |||||||
chr9:128527058 | C | T | 3 | a0002c0002t0002g0226 a0002c0002t0002g0227 a0002c0002t0002g0253 |
3 | HG01256.hp1 HG01517.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1130-121C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128527058 | |||||||
chr9:128527083 | G | A | 1 | a0002c0002t0002g0190 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1130-96G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 7/15 | chr9 | 128527083 | |||||||
chr9:128527321 | G | T | 114 | a0002c0002t0001g0029 a0002c0002t0002g0002 a0002c0002t0002g0011 others(111): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1242+30G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 8/15 | chr9 | 128527321 | |||||||
chr9:128527566 | G | A | 6 | a0001c0001t0001g0065 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG00735.hp1 HG01358.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312+41G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128527566 | |||||||
chr9:128527588 | T | G | 1 | a0002c0002t0002g0235 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1312+63T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128527588 | |||||||
chr9:128527655 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1312+130A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128527655 | |||||||
chr9:128527845 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
171 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.1312+320T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128527845 | |||||||
chr9:128527852 | TACTC | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(20): Show |
26 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1312+329_1312+332d others(6): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128527852 | ||||||
chr9:128527989 | TTTTTTC | T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG00735.hp1 HG01358.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312+470_1312+475d others(8): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128527989 | ||||||
chr9:128528003 | C | CT | 92 | a0001c0001t0001g0098 a0002c0002t0001g0005 a0002c0002t0001g0012 others(89): Show |
98 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.1312+492dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128528003 | ||||||
chr9:128528003 | C | CTT | 36 | a0002c0002t0001g0028 a0002c0002t0002g0167 a0002c0002t0002g0203 others(33): Show |
36 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1312+491_1312+492d others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128528003 | ||||||
chr9:128528030 | T | C | 147 | a0001c0001t0001g0013 a0001c0001t0001g0081 a0001c0001t0001g0099 others(144): Show |
152 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1312+505T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528030 | |||||||
chr9:128528048 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0025 others(21): Show |
27 | HG00733.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1312+523G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528048 | |||||||
chr9:128528092 | C | T | 1 | a0002c0002t0002g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1312+567C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528092 | |||||||
chr9:128528205 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1312+680T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528205 | |||||||
chr9:128528213 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1312+688C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528213 | |||||||
chr9:128528283 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1312+758C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528283 | |||||||
chr9:128528306 | C | CT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0158 others(3): Show |
6 | HG01175.hp1 HG02055.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312+796dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128528306 | ||||||
chr9:128528307 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0153 others(6): Show |
10 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312+782T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528307 | |||||||
chr9:128528365 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0074 |
3 | HG00558.hp2 NA18993.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1312+840G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528365 | |||||||
chr9:128528397 | G | A | 1 | a0002c0002t0003g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1312+872G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528397 | |||||||
chr9:128528494 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1312+969G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528494 | |||||||
chr9:128528600 | G | T | 1 | a0002c0002t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1312+1075G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528600 | |||||||
chr9:128528763 | C | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0088 a0001c0001t0001g0243 others(1): Show |
4 | NA18946.hp1 NA18981.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+1238C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528763 | |||||||
chr9:128528806 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1312+1281G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528806 | |||||||
chr9:128528808 | G | A | 1 | a0002c0002t0002g0197 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1312+1283G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528808 | |||||||
chr9:128528877 | G | A | 1 | a0002c0002t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1312+1352G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528877 | |||||||
chr9:128528878 | A | T | 1 | a0002c0002t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1312+1353A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128528878 | |||||||
chr9:128529049 | G | A | 159 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(156): Show |
165 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1312+1524G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529049 | |||||||
chr9:128529165 | C | T | 1 | a0002c0002t0002g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1312+1640C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529165 | |||||||
chr9:128529202 | C | T | 1 | a0002c0002t0002g0011 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1312+1677C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529202 | |||||||
chr9:128529214 | C | T | 2 | a0001c0001t0001g0301 a0003c0008t0001g0302 |
2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1312+1689C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529214 | |||||||
chr9:128529266 | A | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1312+1741A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529266 | |||||||
chr9:128529375 | G | A | 1 | a0002c0002t0002g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1312+1850G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529375 | |||||||
chr9:128529617 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0085 others(4): Show |
7 | HG00735.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+2092A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529617 | |||||||
chr9:128529693 | TCTCTCTC others(1): Show |
T | 5 | a0002c0002t0002g0019 a0002c0002t0002g0168 a0002c0002t0002g0178 others(2): Show |
5 | HG00673.hp2 HG02080.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312+2184_1312+219 others(12): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128529693 | ||||||
chr9:128529752 | C | T | 6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0268 others(3): Show |
6 | HG02145.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312+2227C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529752 | |||||||
chr9:128529776 | G | A | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1312+2251G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529776 | |||||||
chr9:128529861 | C | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312+2336C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529861 | |||||||
chr9:128529938 | G | A | 1 | a0002c0002t0003g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1312+2413G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529938 | |||||||
chr9:128529990 | A | G | 1 | a0005c0004t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1312+2465A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128529990 | |||||||
chr9:128530087 | T | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.1312+2562T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530087 | |||||||
chr9:128530447 | T | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.1312+2922T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530447 | |||||||
chr9:128530460 | T | A | 6 | a0002c0002t0001g0012 a0002c0002t0001g0024 a0002c0002t0001g0028 others(3): Show |
7 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+2935T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530460 | |||||||
chr9:128530638 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1313-2875G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530638 | |||||||
chr9:128530681 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1313-2832T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530681 | |||||||
chr9:128530802 | C | T | 2 | a0002c0002t0003g0276 a0002c0002t0003g0280 |
2 | NA18942.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1313-2711C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128530802 | |||||||
chr9:128530908 | CA | C | 6 | a0002c0002t0001g0012 a0002c0002t0001g0024 a0002c0002t0001g0028 others(3): Show |
7 | HG01099.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-2591delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128530908 | ||||||
chr9:128531108 | G | A | 97 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0019 others(94): Show |
101 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.1313-2405G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531108 | |||||||
chr9:128531170 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1313-2343C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531170 | |||||||
chr9:128531189 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1313-2324G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531189 | |||||||
chr9:128531214 | C | CA | 22 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0025 others(19): Show |
22 | HG01099.hp2 HG01192.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.1313-2278dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531214 | ||||||
chr9:128531214 | CA | C | 8 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-2278delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531214 | ||||||
chr9:128531289 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1313-2224C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531289 | |||||||
chr9:128531420 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-2093G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531420 | |||||||
chr9:128531525 | C | CA | 10 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0111 others(7): Show |
10 | HG01192.hp2 HG02040.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313-1972dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531525 | ||||||
chr9:128531574 | G | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1313-1939G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531574 | |||||||
chr9:128531721 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1313-1792A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531721 | |||||||
chr9:128531746 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1313-1767C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531746 | |||||||
chr9:128531828 | G | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.1313-1685G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531828 | |||||||
chr9:128531831 | C | CA | 91 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(88): Show |
96 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.1313-1661dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531831 | ||||||
chr9:128531831 | C | CAA | 35 | a0002c0002t0002g0019 a0002c0002t0002g0207 a0002c0002t0002g0235 others(32): Show |
35 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1313-1662_1313-166 others(6): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531831 | ||||||
chr9:128531831 | CA | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0097 others(6): Show |
10 | HG00609.hp1 HG01256.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-1661delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128531831 | ||||||
chr9:128531954 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0162 |
3 | HG02602.hp1 HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1313-1559C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128531954 | |||||||
chr9:128532037 | C | G | 131 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(128): Show |
137 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1313-1476C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532037 | |||||||
chr9:128532124 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1313-1389G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532124 | |||||||
chr9:128532142 | A | ATGCTGTA others(5): Show |
2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1313-1369_1313-135 others(16): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532142 | ||||||
chr9:128532162 | T | C | 1 | a0001c0001t0007g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1313-1351T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532162 | |||||||
chr9:128532164 | G | C | 2 | a0002c0002t0002g0177 a0002c0002t0002g0190 |
2 | HG02155.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1313-1349G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532164 | |||||||
chr9:128532209 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0003g0299 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1313-1286_1313-127 others(14): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | C | CTTTTTTT others(4): Show |
6 | a0002c0002t0003g0283 a0002c0002t0003g0284 a0002c0002t0003g0290 others(3): Show |
6 | HG01975.hp1 NA18949.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-1287_1313-127 others(15): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | C | CTTTTTTT others(5): Show |
14 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(11): Show |
14 | HG01099.hp2 HG01361.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.1313-1288_1313-127 others(16): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | C | CTTTTTTT others(6): Show |
6 | a0002c0002t0003g0278 a0002c0002t0003g0280 a0002c0002t0003g0282 others(3): Show |
6 | HG00609.hp1 HG02040.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-1289_1313-127 others(17): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0003g0292 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1313-1291_1313-127 others(19): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | CT | C | 50 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0025 others(47): Show |
50 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1313-1277delT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | CTT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
134 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.1313-1278_1313-127 others(6): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | CTTT | C | 27 | a0002c0002t0001g0021 a0002c0002t0001g0238 a0002c0002t0001g0239 others(24): Show |
27 | HG00280.hp1 HG00673.hp2 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.1313-1279_1313-127 others(7): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532209 | CTTTT | C | 104 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0024 others(101): Show |
110 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.1313-1280_1313-127 others(8): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532209 | ||||||
chr9:128532421 | T | C | 1 | a0001c0001t0008g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1313-1092T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532421 | |||||||
chr9:128532541 | TAAAG | T | 3 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 |
3 | HG00280.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1313-968_1313-965d others(6): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128532541 | ||||||
chr9:128532695 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1313-818C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532695 | |||||||
chr9:128532827 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1313-686A>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532827 | |||||||
chr9:128532852 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1313-661T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128532852 | |||||||
chr9:128533314 | C | A | 1 | a0002c0002t0002g0320 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1313-199C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128533314 | |||||||
chr9:128533325 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0271 |
2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1313-188G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128533325 | |||||||
chr9:128533418 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1313-95A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128533418 | |||||||
chr9:128533427 | CA | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
182 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(179): Show |
intron_variant | MODIFIER | c.1313-61delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128533427 | ||||||
chr9:128533427 | CAA | C | 146 | a0001c0001t0001g0055 a0001c0001t0001g0087 a0001c0001t0001g0123 others(143): Show |
150 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1313-62_1313-61del others(2): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128533427 | ||||||
chr9:128533427 | CAAA | C | 8 | a0002c0002t0002g0191 a0002c0002t0002g0227 a0002c0002t0002g0228 others(5): Show |
8 | HG00609.hp1 HG01517.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-63_1313-61del others(3): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128533427 | ||||||
chr9:128533427 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1313-76_1313-61del others(16): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr9 | 128533427 | ||||||
chr9:128533430 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0248 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1313-83A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 9/15 | chr9 | 128533430 | |||||||
chr9:128534128 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1646+177G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534128 | |||||||
chr9:128534301 | G | A | 132 | a0001c0001t0001g0266 a0002c0002t0001g0005 a0002c0002t0001g0012 others(129): Show |
138 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1646+350G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534301 | |||||||
chr9:128534386 | T | A | 4 | a0002c0002t0002g0310 a0002c0002t0002g0314 a0002c0002t0002g0315 others(1): Show |
4 | HG02165.hp2 NA18970.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646+435T>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534386 | |||||||
chr9:128534411 | AC | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
158 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1646+461delC | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534411 | |||||||
chr9:128534475 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1646+524T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534475 | |||||||
chr9:128534567 | A | G | 2 | a0002c0002t0002g0311 a0002c0002t0002g0322 |
2 | NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1646+616A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534567 | |||||||
chr9:128534593 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1646+642A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534593 | |||||||
chr9:128534705 | A | G | 2 | a0002c0002t0003g0285 a0002c0002t0003g0288 |
2 | HG00609.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1646+754A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534705 | |||||||
chr9:128534739 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1646+788G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534739 | |||||||
chr9:128534745 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1646+794G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534745 | |||||||
chr9:128534774 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1646+823A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534774 | |||||||
chr9:128534961 | C | T | 10 | a0002c0002t0003g0159 a0002c0002t0003g0292 a0002c0002t0003g0293 others(7): Show |
10 | HG01099.hp2 HG01975.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1646+1010C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534961 | |||||||
chr9:128534964 | G | A | 4 | a0001c0001t0001g0263 a0002c0002t0002g0185 a0002c0002t0002g0196 others(1): Show |
4 | HG03540.hp2 NA18968.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646+1013G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128534964 | |||||||
chr9:128535071 | G | GCATAAAA others(6): Show |
5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646+1121_1646+112 others(17): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr9 | 128535071 | ||||||
chr9:128535077 | A | AAAAGTAA others(5): Show |
1 | a0001c0001t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1646+1127_1646+113 others(16): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr9 | 128535077 | ||||||
chr9:128535281 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1647-1074G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535281 | |||||||
chr9:128535481 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1647-874C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535481 | |||||||
chr9:128535522 | C | CA | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
291 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(288): Show |
intron_variant | MODIFIER | c.1647-817dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr9 | 128535522 | ||||||
chr9:128535522 | C | CAA | 47 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0037 others(44): Show |
47 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1647-818_1647-817d others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr9 | 128535522 | ||||||
chr9:128535539 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1647-816G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535539 | |||||||
chr9:128535541 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1647-814C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535541 | |||||||
chr9:128535589 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0167 others(37): Show |
44 | HG00280.hp2 HG01433.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.1647-766G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535589 | |||||||
chr9:128535681 | G | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1647-674G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535681 | |||||||
chr9:128535744 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1647-611C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535744 | |||||||
chr9:128535850 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647-505C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535850 | |||||||
chr9:128535914 | T | C | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1647-441T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535914 | |||||||
chr9:128535920 | G | A | 1 | a0002c0002t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1647-435G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535920 | |||||||
chr9:128535934 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0131 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-421C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128535934 | |||||||
chr9:128535965 | C | CTT | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.1647-389_1647-388i others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr9 | 128535965 | ||||||
chr9:128536283 | C | T | 1 | a0002c0002t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1647-72C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128536283 | |||||||
chr9:128536311 | A | G | 159 | a0002c0002t0001g0005 a0002c0002t0001g0012 a0002c0002t0001g0021 others(156): Show |
165 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1647-44A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 11/15 | chr9 | 128536311 | |||||||
chr9:128536583 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1776+99C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536583 | |||||||
chr9:128536727 | A | G | 9 | a0002c0002t0001g0021 a0002c0002t0001g0236 a0002c0002t0001g0237 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1776+243A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536727 | |||||||
chr9:128536756 | A | G | 2 | a0002c0002t0002g0172 a0002c0002t0002g0202 |
2 | HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1776+272A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536756 | |||||||
chr9:128536836 | C | T | 1 | a0002c0002t0002g0309 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1776+352C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536836 | |||||||
chr9:128536949 | C | T | 177 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0055 others(174): Show |
183 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1776+465C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536949 | |||||||
chr9:128536961 | G | A | 1 | a0002c0002t0002g0204 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1776+477G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128536961 | |||||||
chr9:128537002 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1776+518T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537002 | |||||||
chr9:128537133 | G | T | 2 | a0002c0002t0002g0331 a0002c0002t0002g0332 |
2 | NA18986.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1776+649G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537133 | |||||||
chr9:128537410 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1777-576G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537410 | |||||||
chr9:128537453 | C | CA | 123 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0062 others(120): Show |
129 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1777-508dupA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr9 | 128537453 | ||||||
chr9:128537453 | C | CAA | 11 | a0001c0001t0001g0274 a0002c0002t0001g0238 a0002c0002t0001g0240 others(8): Show |
11 | HG01433.hp2 HG02027.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1777-509_1777-508d others(4): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr9 | 128537453 | ||||||
chr9:128537453 | CA | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0067 others(11): Show |
14 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1777-508delA | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr9 | 128537453 | ||||||
chr9:128537453 | CAAAAAAA others(6): Show |
C | 29 | a0002c0002t0002g0215 a0002c0002t0003g0015 a0002c0002t0003g0159 others(26): Show |
29 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1777-520_1777-508d others(15): Show |
GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr9 | 128537453 | ||||||
chr9:128537659 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1777-327A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537659 | |||||||
chr9:128537789 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(57): Show |
64 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1777-197A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537789 | |||||||
chr9:128537864 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
158 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1777-122G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537864 | |||||||
chr9:128537880 | G | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1777-106G>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537880 | |||||||
chr9:128537957 | C | G | 1 | a0002c0002t0002g0207 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1777-29C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 12/15 | chr9 | 128537957 | |||||||
chr9:128538163 | G | A | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1881+73G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538163 | |||||||
chr9:128538260 | T | C | 2 | a0002c0002t0002g0319 a0002c0002t0002g0327 |
2 | HG01433.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1881+170T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538260 | |||||||
chr9:128538267 | A | G | 40 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0167 others(37): Show |
44 | HG00280.hp2 HG01433.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.1881+177A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538267 | |||||||
chr9:128538313 | C | T | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1881+223C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538313 | |||||||
chr9:128538354 | G | A | 4 | a0002c0002t0002g0310 a0002c0002t0002g0314 a0002c0002t0002g0315 others(1): Show |
4 | HG02165.hp2 NA18970.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+264G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538354 | |||||||
chr9:128538384 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1881+294C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538384 | |||||||
chr9:128538481 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1881+391T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538481 | |||||||
chr9:128538553 | T | C | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG01358.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1881+463T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538553 | |||||||
chr9:128538652 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
113 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(110): Show |
intron_variant | MODIFIER | c.1881+562C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538652 | |||||||
chr9:128538755 | G | GT | 3 | a0001c0001t0001g0013 a0001c0001t0001g0264 a0001c0001t0001g0272 |
4 | HG02559.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+666dupT | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr9 | 128538755 | ||||||
chr9:128538767 | C | T | 1 | a0002c0002t0002g0225 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1881+677C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538767 | |||||||
chr9:128538854 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1882-762C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128538854 | |||||||
chr9:128539033 | G | C | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1882-583G>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539033 | |||||||
chr9:128539204 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1882-412A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539204 | |||||||
chr9:128539225 | C | A | 1 | a0002c0002t0002g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1882-391C>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539225 | |||||||
chr9:128539275 | A | T | 1 | a0002c0002t0002g0318 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1882-341A>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539275 | |||||||
chr9:128539372 | T | C | 129 | a0002c0002t0001g0012 a0002c0002t0001g0021 a0002c0002t0001g0024 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1882-244T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539372 | |||||||
chr9:128539480 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1882-136G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539480 | |||||||
chr9:128539495 | G | A | 2 | a0002c0002t0002g0175 a0002c0002t0002g0200 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1882-121G>A | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 13/15 | chr9 | 128539495 | |||||||
chr9:128540215 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1965-60C>T | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 14/15 | chr9 | 128540215 | |||||||
chr9:128540478 | C | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2028+140C>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 15/15 | chr9 | 128540478 | |||||||
chr9:128540521 | A | G | 6 | a0002c0002t0002g0185 a0002c0002t0002g0196 a0002c0002t0002g0197 others(3): Show |
6 | NA18945.hp2 NA18968.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028+183A>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 15/15 | chr9 | 128540521 | |||||||
chr9:128540679 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0121 |
2 | NA19003.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2028+341T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 15/15 | chr9 | 128540679 | |||||||
chr9:128540757 | T | C | 28 | a0002c0002t0003g0015 a0002c0002t0003g0159 a0002c0002t0003g0275 others(25): Show |
28 | HG00609.hp1 HG01099.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.2029-345T>C | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 15/15 | chr9 | 128540757 | |||||||
chr9:128541029 | T | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0245 |
3 | HG02055.hp1 HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2029-73T>G | GLE1 | ENSG00000119392.16 | transcript | ENST00000309971.9 | protein_coding | 15/15 | chr9 | 128541029 |