geneid | 92906 |
---|---|
ensemblid | ENSG00000143889.16 |
hgncid | 25127 |
symbol | HNRNPLL |
name | heterogeneous nuclear ribonucleoprotein L like |
refseq_nuc | NM_138394.4 |
refseq_prot | NP_612403.2 |
ensembl_nuc | ENST00000449105.8 |
ensembl_prot | ENSP00000390625.3 |
mane_status | MANE Select |
chr | chr2 |
start | 38561969 |
end | 38602928 |
strand | - |
ver | v1.2 |
region | chr2:38561969-38602928 |
region5000 | chr2:38556969-38607928 |
regionname0 | HNRNPLL_chr2_38561969_38602928 |
regionname5000 | HNRNPLL_chr2_38556969_38607928 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 542 | 316 | 87 | 60 | 121 | 12 | 34 | 87 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0002 | 0/0 | 543 | 11 | 3 | 0 | 8 | 0 | 0 | 8 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0003 | 0/0 | 542 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0004 | 0/0 | 542 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1629 | 315 | 87 | 59 | 121 | 12 | 34 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
c0002 | 0/0 | 1632 | 11 | 3 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
c0003 | 0/0 | 1629 | 9 | 0 | 0 | 9 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
c0004 | 0/0 | 1629 | 2 | 0 | 0 | 0 | 2 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
c0005 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2516 | 167 | 26 | 39 | 67 | 8 | 25 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0002 | 0/0 | 2516 | 57 | 25 | 8 | 24 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0003 | 0/0 | 2516 | 30 | 9 | 1 | 15 | 3 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0004 | 0/0 | 2516 | 20 | 1 | 2 | 13 | 1 | 3 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0005 | 0/0 | 2516 | 10 | 1 | 7 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0006 | 0/0 | 2516 | 8 | 0 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0007 | 0/0 | 2516 | 6 | 6 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0008 | 0/0 | 2516 | 5 | 0 | 0 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0009 | 0/0 | 2516 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0010 | 0/0 | 2516 | 5 | 4 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0011 | 0/0 | 2516 | 4 | 3 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0012 | 0/0 | 2516 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0013 | 0/0 | 2516 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0014 | 0/0 | 2516 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0015 | 0/0 | 2516 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0016 | 0/0 | 2516 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0017 | 0/0 | 2516 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0018 | 0/0 | 2516 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0019 | 0/0 | 2516 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0020 | 0/0 | 2516 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0021 | 0/0 | 2516 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0022 | 0/0 | 2516 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0023 | 0/0 | 2516 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
t0024 | 0/0 | 2516 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 0 | 3 | 10 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0011 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1629 | 315 | 87 | 59 | 121 | 12 | 34 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0005 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0002c0002 | 0/0 | 1632 | 11 | 3 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0003c0003 | 0/0 | 1629 | 9 | 0 | 0 | 9 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0004c0004 | 0/0 | 1629 | 2 | 0 | 0 | 0 | 2 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4144 | 164 | 26 | 38 | 67 | 6 | 25 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0002 | 0/0 | 4144 | 57 | 25 | 8 | 24 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0003 | 0/0 | 4144 | 30 | 9 | 1 | 15 | 3 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0004 | 0/0 | 4144 | 11 | 1 | 2 | 4 | 1 | 3 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0005 | 0/0 | 4144 | 10 | 1 | 7 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0007 | 0/0 | 4144 | 6 | 6 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0008 | 0/0 | 4144 | 5 | 0 | 0 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0009 | 0/0 | 4144 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0010 | 0/0 | 4144 | 5 | 4 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0011 | 0/0 | 4144 | 4 | 3 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0012 | 0/0 | 4144 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0014 | 0/0 | 4144 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0015 | 0/0 | 4144 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0016 | 0/0 | 4144 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0017 | 0/0 | 4144 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0018 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0019 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0020 | 0/0 | 4144 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0021 | 0/0 | 4144 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0022 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0023 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0001t0024 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0001c0005t0001 | 0/0 | 4144 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0002c0002t0006 | 0/0 | 4147 | 8 | 0 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0002c0002t0013 | 0/0 | 4147 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0003c0003t0004 | 0/0 | 4144 | 9 | 0 | 0 | 9 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
a0004c0004t0001 | 0/0 | 4144 | 2 | 0 | 0 | 0 | 2 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | copy fasta | chr2 | 38556969 | 38607928 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 0 | 3 | 10 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0011 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0010g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0011g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0011g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0012g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0015g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0015g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0016g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0018g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0020g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0021g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0023g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0001t0024g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0001c0005t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0002c0002t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0003c0003t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0003c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0003c0003t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0003c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0004c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01192 | hp1 | a0001 | c0005 | t0001 | g0145 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01258 | hp2 | a0001 | c0001 | t0015 | g0202 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0223 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01496 | hp1 | a0001 | c0001 | t0010 | g0029 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01515 | hp1 | a0004 | c0004 | t0001 | g0263 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01884 | hp2 | a0001 | c0001 | t0023 | g0046 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02129 | hp2 | a0001 | c0001 | t0012 | g0154 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02155 | hp1 | a0001 | c0001 | t0020 | g0076 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0233 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02818 | hp2 | a0001 | c0001 | t0022 | g0035 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0157 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02922 | hp1 | a0001 | c0001 | t0016 | g0102 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03139 | hp2 | a0001 | c0001 | t0024 | g0064 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03540 | hp2 | a0001 | c0001 | t0018 | g0108 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0168 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03669 | hp2 | a0001 | c0001 | t0017 | g0196 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04184 | hp1 | a0001 | c0001 | t0014 | g0111 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG04204 | hp2 | a0001 | c0001 | t0014 | g0094 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18522 | hp2 | a0001 | c0001 | t0011 | g0222 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18906 | hp1 | a0002 | c0002 | t0013 | g0252 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0177 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18945 | hp2 | a0002 | c0002 | t0006 | g0257 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18950 | hp1 | a0002 | c0002 | t0006 | g0262 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18951 | hp1 | a0001 | c0001 | t0012 | g0134 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18951 | hp2 | a0002 | c0002 | t0006 | g0255 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18957 | hp2 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18960 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18974 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18980 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18980 | hp2 | a0001 | c0001 | t0012 | g0114 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18988 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18994 | hp2 | a0002 | c0002 | t0006 | g0260 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18999 | hp2 | a0001 | c0001 | t0021 | g0242 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19003 | hp1 | a0001 | c0001 | t0008 | g0198 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19003 | hp2 | a0002 | c0002 | t0006 | g0258 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19030 | hp2 | a0002 | c0002 | t0013 | g0254 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19043 | hp2 | a0002 | c0002 | t0013 | g0253 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19060 | hp1 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19060 | hp2 | a0003 | c0003 | t0004 | g0248 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19062 | hp1 | a0003 | c0003 | t0004 | g0245 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19063 | hp2 | a0002 | c0002 | t0006 | g0261 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19068 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19079 | hp1 | a0002 | c0002 | t0006 | g0256 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19084 | hp1 | a0002 | c0002 | t0006 | g0259 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19087 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19088 | hp2 | a0003 | c0003 | t0004 | g0249 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0241 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ASW | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20752 | hp2 | a0004 | c0004 | t0001 | g0264 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0012 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20805 | hp2 | a0001 | c0001 | t0015 | g0189 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0028 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA20300 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0147 | REF | REF | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38561969
|
T | G | 1 | a0002 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
splice_region_variant | LOW | c.*2213A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | chr2 | 38561969 | ||||||
chr2:38582079
|
T | C | 1 | a0003 | 9 | NA18957.hp2 NA18960.hp1 NA18974.hp1 others(6): Show |
missense_variant | MODERATE | c.722A>G | p.Tyr241Cys | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/13 | 1024/4144 | 722/1629 | 241/542 | chr2 | 38582079 | ||
chr2:38602455
|
G | GGCC | 1 | a0002 | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
conservative_inframe_insertion | MODERATE | c.169_171dupGGC | p.Gly57dup | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/13 | 473/4144 | 171/1629 | 57/542 | chr2 | 38602455 | ||
chr2:38602595
|
G | A | 1 | a0004 | 2 | HG01515.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.32C>T | p.Thr11Met | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/13 | 334/4144 | 32/1629 | 11/542 | chr2 | 38602595 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38569136
|
T | C | 1 | a0001c0005 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1413A>G | p.Thr471Thr | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/13 | 1715/4144 | 1413/1629 | 471/542 | chr2 | 38569136 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38561994
|
A | G | 1 | a0001c0001t0016 | 2 | HG02630.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2188 | chr2 | 38561994 | |||||
chr2:38562039
|
A | G | 1 | a0001c0001t0005 | 10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2143T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2143 | chr2 | 38562039 | |||||
chr2:38562043
|
T | A | 1 | a0001c0001t0015 | 2 | HG01258.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2139A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2139 | chr2 | 38562043 | |||||
chr2:38562049
|
T | A | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0020others(2): Show | 47 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2133A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2133 | chr2 | 38562049 | |||||
chr2:38562101
|
T | C | 3 | a0001c0001t0004a0001c0001t0021a0003c0003t0004 | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2081A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2081 | chr2 | 38562101 | |||||
chr2:38562103
|
G | T | 1 | a0001c0001t0021 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2079 | chr2 | 38562103 | |||||
chr2:38562163
|
G | C | 1 | a0001c0001t0020 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2019C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2019 | chr2 | 38562163 | |||||
chr2:38562351
|
T | C | 1 | a0001c0001t0007 | 6 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1831A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1831 | chr2 | 38562351 | |||||
chr2:38562366
|
T | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 152 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1816A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1816 | chr2 | 38562366 | |||||
chr2:38562383
|
A | G | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0021others(2): Show | 33 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1799T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1799 | chr2 | 38562383 | |||||
chr2:38562540
|
A | G | 3 | a0001c0001t0003a0001c0001t0009a0001c0001t0020 | 36 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1642T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1642 | chr2 | 38562540 | |||||
chr2:38562545
|
T | G | 1 | a0002c0002t0006 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1637A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1637 | chr2 | 38562545 | |||||
chr2:38562643
|
C | A | 1 | a0001c0001t0022 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1539 | chr2 | 38562643 | |||||
chr2:38562850
|
C | T | 1 | a0001c0001t0014 | 2 | HG04184.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1332G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1332 | chr2 | 38562850 | |||||
chr2:38562976
|
A | G | 2 | a0001c0001t0009a0001c0001t0019 | 6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1206T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1206 | chr2 | 38562976 | |||||
chr2:38562980
|
C | T | 1 | a0002c0002t0006 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1202G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1202 | chr2 | 38562980 | |||||
chr2:38563161
|
C | T | 1 | a0001c0001t0018 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1021 | chr2 | 38563161 | |||||
chr2:38563269
|
C | T | 1 | a0001c0001t0017 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 913 | chr2 | 38563269 | |||||
chr2:38563308
|
A | T | 1 | a0001c0001t0008 | 5 | NA18941.hp2 NA18956.hp1 NA19003.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*874T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 874 | chr2 | 38563308 | |||||
chr2:38563373
|
T | G | 1 | a0001c0001t0012 | 4 | HG02129.hp2 NA18951.hp1 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*809A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 809 | chr2 | 38563373 | |||||
chr2:38563630
|
G | A | 1 | a0001c0001t0010 | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 552 | chr2 | 38563630 | |||||
chr2:38563758
|
G | A | 1 | a0001c0001t0023 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 424 | chr2 | 38563758 | |||||
chr2:38563969
|
T | C | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 213 | chr2 | 38563969 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38564304
|
G | C | 15 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(12): Show | 22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1574-67C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564304 | ||||||
chr2:38564391
|
C | T | 1 | a0001c0001t0007g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1574-154G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564391 | ||||||
chr2:38564401
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-164G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564401 | ||||||
chr2:38564451
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1574-214G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564451 | ||||||
chr2:38564613
|
C | CA | 35 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0123others(32): Show | 37 | HG00140.hp1 HG00423.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1574-377dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | ||||||
chr2:38564613
|
C | CAA | 10 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(7): Show | 19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1574-378_1574-377d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | ||||||
chr2:38564613
|
C | CAAA | 6 | a0001c0001t0003g0007a0001c0001t0003g0077a0001c0001t0003g0079others(3): Show | 9 | HG00597.hp1 HG02074.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.1574-379_1574-377d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | ||||||
chr2:38564613
|
C | CAAAA | 8 | a0001c0001t0003g0164a0002c0002t0006g0255a0002c0002t0006g0256others(5): Show | 8 | HG06807.hp1 NA18945.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-380_1574-377d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | ||||||
chr2:38564700
|
T | G | 14 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0037others(11): Show | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1574-463A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564700 | ||||||
chr2:38564725
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-488G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564725 | ||||||
chr2:38564769
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1574-532A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564769 | ||||||
chr2:38564778
|
C | G | 86 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0002g0003others(83): Show | 112 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1574-541G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564778 | ||||||
chr2:38564835
|
A | G | 1 | a0001c0001t0007g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1574-598T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564835 | ||||||
chr2:38564844
|
A | G | 1 | a0001c0001t0007g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1574-607T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564844 | ||||||
chr2:38564903
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1574-666A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564903 | ||||||
chr2:38565004
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-767T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565004 | ||||||
chr2:38565008
|
AC | A | 30 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(27): Show | 43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1574-772delG | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565008 | ||||||
chr2:38565009
|
C | A | 52 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(49): Show | 65 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1574-772G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565009 | ||||||
chr2:38565295
|
A | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-1058T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565295 | ||||||
chr2:38565578
|
A | ATAAGCTG others(4): Show |
1 | a0001c0001t0004g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1574-1352_1574-134 others(15): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565578 | ||||||
chr2:38565594
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1574-1357C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565594 | ||||||
chr2:38565609
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1574-1372G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565609 | ||||||
chr2:38565647
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1574-1410C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565647 | ||||||
chr2:38565662
|
G | A | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1574-1425C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565662 | ||||||
chr2:38565678
|
G | T | 1 | a0001c0001t0009g0157 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1574-1441C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565678 | ||||||
chr2:38565727
|
C | CA | 13 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0093others(10): Show | 13 | HG01192.hp1 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1574-1491dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CA | C | 41 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0104others(38): Show | 51 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1574-1491delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAA | C | 13 | a0001c0001t0001g0098a0001c0001t0001g0141a0001c0001t0001g0182others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1574-1492_1574-149 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAA | C | 12 | a0001c0001t0002g0008a0001c0001t0002g0082a0001c0001t0002g0097others(9): Show | 15 | HG01106.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1574-1493_1574-149 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAAA | C | 6 | a0001c0001t0003g0077a0001c0001t0003g0085a0001c0001t0004g0247others(3): Show | 6 | HG03834.hp2 NA18906.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1574-1494_1574-149 others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAAAA | C | 39 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0007others(36): Show | 58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1574-1495_1574-149 others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAAAAAA | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0001g0208others(3): Show | 7 | HG00544.hp1 HG00639.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1574-1497_1574-149 others(11): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAAAAAA others(1): Show |
C | 50 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0026others(47): Show | 67 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1574-1498_1574-149 others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565727
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0020a0001c0001t0001g0113a0001c0001t0001g0135others(2): Show | 6 | HG00099.hp2 HG00735.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1574-1504_1574-149 others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | ||||||
chr2:38565786
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1574-1549A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565786 | ||||||
chr2:38565856
|
T | C | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1574-1619A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565856 | ||||||
chr2:38565968
|
G | GT | 27 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(24): Show | 39 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1574-1732dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565968 | ||||||
chr2:38566027
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1574-1790A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566027 | ||||||
chr2:38566134
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1574-1897C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566134 | ||||||
chr2:38566323
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+1876C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566323 | ||||||
chr2:38566378
|
A | AAC | 25 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(22): Show | 37 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1573+1820_1573+182 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566378 | ||||||
chr2:38566378
|
A | C | 3 | a0001c0001t0011g0028a0001c0001t0011g0222a0001c0001t0011g0223 | 4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+1821T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566378 | ||||||
chr2:38566379
|
C | A | 3 | a0001c0001t0003g0077a0001c0001t0003g0088a0001c0001t0003g0163 | 3 | HG02055.hp1 HG03471.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1573+1820G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566379 | ||||||
chr2:38566379
|
C | CA | 3 | a0001c0001t0011g0028a0001c0001t0011g0222a0001c0001t0011g0223 | 4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+1819_1573+182 others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566379 | ||||||
chr2:38566380
|
C | A | 29 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(26): Show | 42 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1573+1819G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | ||||||
chr2:38566380
|
C | CA | 30 | a0001c0001t0001g0090a0001c0001t0001g0116a0001c0001t0001g0129others(27): Show | 35 | HG00738.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1573+1818dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | ||||||
chr2:38566380
|
C | CAA | 44 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0150others(41): Show | 55 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1573+1817_1573+181 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | ||||||
chr2:38566380
|
C | CAAA | 14 | a0001c0001t0002g0070a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1573+1816_1573+181 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | ||||||
chr2:38566380
|
C | CCAA | 3 | a0001c0001t0003g0077a0001c0001t0003g0088a0001c0001t0003g0163 | 3 | HG02055.hp1 HG03471.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1573+1818_1573+181 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | ||||||
chr2:38566408
|
G | C | 2 | a0001c0001t0016g0102a0001c0001t0016g0109 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1573+1791C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566408 | ||||||
chr2:38566473
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+1726G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566473 | ||||||
chr2:38566539
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573+1660T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566539 | ||||||
chr2:38566582
|
C | T | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+1617G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566582 | ||||||
chr2:38566790
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1573+1409G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566790 | ||||||
chr2:38566795
|
G | C | 1 | a0001c0001t0022g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1573+1404C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566795 | ||||||
chr2:38566796
|
C | A | 1 | a0001c0001t0022g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1573+1403G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566796 | ||||||
chr2:38566821
|
T | TA | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(6): Show | 11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1573+1377dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566821 | ||||||
chr2:38566844
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1573+1355T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566844 | ||||||
chr2:38566870
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1573+1329C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566870 | ||||||
chr2:38567039
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1573+1160G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567039 | ||||||
chr2:38567067
|
A | T | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1573+1132T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567067 | ||||||
chr2:38567126
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1573+1073G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567126 | ||||||
chr2:38567165
|
G | A | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+1034C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567165 | ||||||
chr2:38567186
|
C | T | 2 | a0001c0001t0016g0102a0001c0001t0016g0109 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1573+1013G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567186 | ||||||
chr2:38567224
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573+975A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567224 | ||||||
chr2:38567225
|
C | T | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0239others(1): Show | 6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1573+974G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567225 | ||||||
chr2:38567236
|
G | C | 1 | a0001c0001t0002g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1573+963C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567236 | ||||||
chr2:38567245
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1573+954T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567245 | ||||||
chr2:38567269
|
A | AT | 23 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(20): Show | 36 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1573+929dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567269 | ||||||
chr2:38567353
|
C | T | 1 | a0002c0002t0006g0261 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1573+846G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567353 | ||||||
chr2:38567430
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0142 | 3 | HG03942.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1573+769A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567430 | ||||||
chr2:38567472
|
G | C | 1 | a0001c0001t0005g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1573+727C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567472 | ||||||
chr2:38567481
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+718A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567481 | ||||||
chr2:38567575
|
G | A | 19 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(16): Show | 31 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573+624C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567575 | ||||||
chr2:38567823
|
A | C | 1 | a0001c0001t0002g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1573+376T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567823 | ||||||
chr2:38567937
|
T | C | 2 | a0001c0001t0007g0099a0001c0001t0018g0108 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1573+262A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567937 | ||||||
chr2:38568044
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1573+155T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38568044 | ||||||
chr2:38568083
|
T | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0002g0166others(2): Show | 7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573+116A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38568083 | ||||||
chr2:38568374
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0216 | 3 | NA18979.hp1 NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1474+12G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 11/12 | chr2 | 38568374 | ||||||
chr2:38568536
|
T | C | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0239others(1): Show | 6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-93A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568536 | ||||||
chr2:38568614
|
A | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0017g0196 | 3 | HG03492.hp2 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1417-171T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568614 | ||||||
chr2:38568726
|
G | A | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-283C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568726 | ||||||
chr2:38568823
|
G | C | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416+310C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568823 | ||||||
chr2:38568860
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1416+273A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568860 | ||||||
chr2:38568971
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1416+162T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568971 | ||||||
chr2:38569061
|
A | C | 3 | a0001c0001t0002g0065a0001c0001t0002g0068a0001c0001t0002g0070 | 3 | HG03139.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1416+72T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38569061 | ||||||
chr2:38569120
|
T | C | 8 | a0001c0001t0007g0078a0001c0001t0007g0099a0001c0001t0007g0148others(5): Show | 8 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416+13A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38569120 | ||||||
chr2:38569423
|
A | G | 1 | a0001c0001t0016g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1215-89T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569423 | ||||||
chr2:38569483
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1215-149A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569483 | ||||||
chr2:38569542
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0002g0166others(2): Show | 7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215-208A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569542 | ||||||
chr2:38569621
|
C | T | 2 | a0001c0001t0002g0234a0001c0001t0002g0236 | 2 | HG00738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1214+183G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569621 | ||||||
chr2:38569751
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0113a0001c0001t0001g0135others(2): Show | 6 | HG00099.hp2 HG00735.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1214+53C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569751 | ||||||
chr2:38569978
|
A | C | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-53T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38569978 | ||||||
chr2:38570054
|
T | TG | 19 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(16): Show | 31 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1093-130dupC | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570054 | ||||||
chr2:38570100
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1093-175T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570100 | ||||||
chr2:38570134
|
C | A | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-209G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570134 | ||||||
chr2:38570161
|
T | C | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-236A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570161 | ||||||
chr2:38570193
|
T | C | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1093-268A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570193 | ||||||
chr2:38570232
|
A | G | 36 | a0001c0001t0002g0008a0001c0001t0002g0082a0001c0001t0002g0095others(33): Show | 46 | HG00140.hp2 HG00423.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1093-307T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570232 | ||||||
chr2:38570345
|
T | C | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-420A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570345 | ||||||
chr2:38570468
|
G | C | 1 | a0001c0001t0004g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1093-543C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570468 | ||||||
chr2:38570493
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1093-568A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570493 | ||||||
chr2:38570587
|
T | C | 26 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(23): Show | 37 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1093-662A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570587 | ||||||
chr2:38570864
|
G | C | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-939C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570864 | ||||||
chr2:38570879
|
C | CA | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(5): Show | 10 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1093-955dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570879 | ||||||
chr2:38570918
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1093-993A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570918 | ||||||
chr2:38570945
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG00639.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1093-1020C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570945 | ||||||
chr2:38571145
|
T | C | 19 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(16): Show | 30 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1093-1220A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571145 | ||||||
chr2:38571200
|
G | GTTTAA | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-1276_1093-127 others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571200 | ||||||
chr2:38571304
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1093-1379T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571304 | ||||||
chr2:38571346
|
CAGTG | C | 15 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(12): Show | 22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1093-1425_1093-142 others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571346 | ||||||
chr2:38571352
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1093-1427C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571352 | ||||||
chr2:38571434
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1093-1509A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571434 | ||||||
chr2:38571461
|
G | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1093-1536C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571461 | ||||||
chr2:38571980
|
G | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0002g0166others(2): Show | 7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+1230C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571980 | ||||||
chr2:38572096
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1092+1114T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572096 | ||||||
chr2:38572212
|
A | ATGTTT | 105 | a0001c0001t0001g0047a0001c0001t0001g0165a0001c0001t0001g0170others(102): Show | 140 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.1092+993_1092+997d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572212 | ||||||
chr2:38572212
|
A | ATGTTTTG others(3): Show |
2 | a0001c0001t0002g0015a0001c0001t0011g0223 | 3 | HG00558.hp2 HG00621.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1092+988_1092+997d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572212 | ||||||
chr2:38572341
|
A | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+869T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572341 | ||||||
chr2:38572400
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0079a0001c0001t0003g0083others(1): Show | 7 | HG00597.hp1 HG02074.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+810A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572400 | ||||||
chr2:38572410
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1092+800T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572410 | ||||||
chr2:38572414
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0056a0001c0001t0002g0060others(1): Show | 5 | NA18943.hp2 NA18986.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+796T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572414 | ||||||
chr2:38572493
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0002g0166others(2): Show | 7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+717A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572493 | ||||||
chr2:38572622
|
T | C | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+588A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572622 | ||||||
chr2:38572678
|
G | A | 100 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0014others(97): Show | 132 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1092+532C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572678 | ||||||
chr2:38572695
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+515A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572695 | ||||||
chr2:38572729
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0115 | 2 | NA18970.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1092+481C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572729 | ||||||
chr2:38572754
|
G | A | 37 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0014others(34): Show | 48 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1092+456C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572754 | ||||||
chr2:38572884
|
C | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+326G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572884 | ||||||
chr2:38572902
|
A | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+308T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572902 | ||||||
chr2:38573192
|
A | G | 19 | a0001c0001t0001g0162a0001c0001t0002g0095a0001c0001t0004g0032others(16): Show | 27 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1092+18T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38573192 | ||||||
chr2:38573462
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.875-35G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573462 | ||||||
chr2:38573549
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.875-122A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573549 | ||||||
chr2:38573671
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-244G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573671 | ||||||
chr2:38573735
|
C | T | 12 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(9): Show | 15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.875-308G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573735 | ||||||
chr2:38574105
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(180): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.875-678A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574105 | ||||||
chr2:38574140
|
A | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.875-713T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574140 | ||||||
chr2:38574166
|
A | G | 2 | a0001c0001t0007g0152a0001c0001t0007g0168 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.875-739T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574166 | ||||||
chr2:38574318
|
A | T | 8 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0039others(5): Show | 10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.875-891T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574318 | ||||||
chr2:38574437
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.875-1010A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574437 | ||||||
chr2:38574549
|
CTAAG | C | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-1126_875-1123d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574549 | ||||||
chr2:38575018
|
C | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1591G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575018 | ||||||
chr2:38575022
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.875-1595A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575022 | ||||||
chr2:38575203
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1776T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575203 | ||||||
chr2:38575235
|
TA | T | 2 | a0001c0001t0009g0023a0001c0001t0009g0158 | 3 | HG02717.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.875-1809delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575235 | ||||||
chr2:38575300
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.875-1873A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575300 | ||||||
chr2:38575325
|
A | T | 3 | a0001c0001t0011g0028a0001c0001t0011g0222a0001c0001t0011g0223 | 4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1898T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575325 | ||||||
chr2:38575360
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.875-1933T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575360 | ||||||
chr2:38575578
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.874+1883T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575578 | ||||||
chr2:38575590
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.874+1871C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575590 | ||||||
chr2:38575599
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0097 | 4 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+1862G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575599 | ||||||
chr2:38575655
|
C | A | 1 | a0001c0001t0007g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.874+1806G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575655 | ||||||
chr2:38575724
|
G | A | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.874+1737C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575724 | ||||||
chr2:38575760
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1701C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575760 | ||||||
chr2:38575779
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.874+1682A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575779 | ||||||
chr2:38575939
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1522T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575939 | ||||||
chr2:38576205
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1256A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576205 | ||||||
chr2:38576268
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.874+1193T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576268 | ||||||
chr2:38576307
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.874+1154G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576307 | ||||||
chr2:38576360
|
C | G | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(5): Show | 10 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.874+1101G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576360 | ||||||
chr2:38576577
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.874+884G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576577 | ||||||
chr2:38576673
|
T | C | 20 | a0001c0001t0001g0162a0001c0001t0002g0055a0001c0001t0002g0095others(17): Show | 28 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.874+788A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576673 | ||||||
chr2:38576713
|
T | A | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.874+748A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576713 | ||||||
chr2:38576777
|
G | A | 2 | a0001c0001t0016g0102a0001c0001t0016g0109 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.874+684C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576777 | ||||||
chr2:38576989
|
C | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0014a0001c0001t0002g0015others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.874+472G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576989 | ||||||
chr2:38577082
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.874+379A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577082 | ||||||
chr2:38577311
|
A | C | 20 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(17): Show | 32 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.874+150T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577311 | ||||||
chr2:38577334
|
G | A | 2 | a0001c0001t0003g0079a0001c0001t0003g0083 | 2 | NA18943.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.874+127C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577334 | ||||||
chr2:38577647
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803-115G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577647 | ||||||
chr2:38577671
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.803-139G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577671 | ||||||
chr2:38577944
|
A | G | 1 | a0001c0001t0011g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.803-412T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577944 | ||||||
chr2:38578058
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.803-526G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578058 | ||||||
chr2:38578143
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.803-611G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578143 | ||||||
chr2:38578407
|
G | C | 1 | a0001c0001t0004g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.803-875C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578407 | ||||||
chr2:38578444
|
A | G | 1 | a0001c0001t0004g0033 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.803-912T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578444 | ||||||
chr2:38578454
|
C | T | 111 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0014others(108): Show | 145 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.803-922G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578454 | ||||||
chr2:38578467
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.803-935T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578467 | ||||||
chr2:38578643
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.803-1111G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578643 | ||||||
chr2:38578881
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-1349G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578881 | ||||||
chr2:38579037
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.803-1505A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579037 | ||||||
chr2:38579040
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803-1508C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579040 | ||||||
chr2:38579068
|
T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.803-1536A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579068 | ||||||
chr2:38579090
|
C | A | 1 | a0001c0001t0001g0027 | 2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.803-1558G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579090 | ||||||
chr2:38579148
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-1616A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579148 | ||||||
chr2:38579159
|
G | C | 1 | a0001c0001t0002g0060 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.803-1627C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579159 | ||||||
chr2:38579187
|
A | C | 47 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0170others(44): Show | 59 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1655T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579187 | ||||||
chr2:38579380
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1848C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579380 | ||||||
chr2:38579390
|
C | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1858G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579390 | ||||||
chr2:38579391
|
CTAAAACT others(1): Show |
C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1867_803-1860d others(10): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579391 | ||||||
chr2:38579417
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.803-1885T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579417 | ||||||
chr2:38579441
|
T | C | 1 | a0001c0001t0012g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1909A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579441 | ||||||
chr2:38579489
|
G | A | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.803-1957C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579489 | ||||||
chr2:38579507
|
G | A | 12 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(9): Show | 15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-1975C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579507 | ||||||
chr2:38579715
|
G | A | 17 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(14): Show | 29 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.803-2183C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579715 | ||||||
chr2:38579725
|
TTTTAAAA others(9): Show |
T | 1 | a0002c0002t0006g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.802+2172_802+2187d others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579725 | ||||||
chr2:38579729
|
A | T | 2 | a0001c0001t0018g0108a0001c0001t0019g0175 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.802+2184T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579729 | ||||||
chr2:38579741
|
A | AT | 99 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0150others(96): Show | 133 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.802+2171dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579741 | ||||||
chr2:38579741
|
A | ATT | 7 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(4): Show | 7 | NA18945.hp2 NA18951.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+2170_802+2171d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579741 | ||||||
chr2:38579750
|
G | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0095 | 2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2163C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579750 | ||||||
chr2:38579752
|
T | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0095 | 2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2161A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579752 | ||||||
chr2:38579754
|
A | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0095 | 2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2159T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579754 | ||||||
chr2:38579884
|
A | G | 24 | a0001c0001t0001g0162a0001c0001t0002g0095a0001c0001t0004g0032others(21): Show | 32 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.802+2029T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579884 | ||||||
chr2:38580035
|
C | G | 40 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0014others(37): Show | 51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.802+1878G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580035 | ||||||
chr2:38580059
|
C | T | 11 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232others(8): Show | 11 | HG02647.hp1 HG03130.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.802+1854G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580059 | ||||||
chr2:38580131
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.802+1782A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580131 | ||||||
chr2:38580164
|
A | T | 15 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232others(12): Show | 16 | HG02647.hp1 HG02717.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+1749T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580164 | ||||||
chr2:38580236
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.802+1677C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580236 | ||||||
chr2:38580299
|
G | A | 32 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(29): Show | 45 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.802+1614C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580299 | ||||||
chr2:38580301
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.802+1612G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580301 | ||||||
chr2:38580555
|
T | C | 2 | a0001c0001t0001g0144a0001c0005t0001g0145 | 2 | HG01192.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.802+1358A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580555 | ||||||
chr2:38580764
|
G | A | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.802+1149C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580764 | ||||||
chr2:38580874
|
T | C | 1 | a0001c0001t0005g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.802+1039A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580874 | ||||||
chr2:38580893
|
T | C | 14 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(11): Show | 25 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+1020A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580893 | ||||||
chr2:38580968
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802+945G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580968 | ||||||
chr2:38581115
|
G | C | 1 | a0001c0001t0002g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+798C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581115 | ||||||
chr2:38581652
|
GA | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0017g0196 | 3 | HG03492.hp2 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.802+260delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581652 | ||||||
chr2:38581715
|
A | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+198T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581715 | ||||||
chr2:38581744
|
A | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.802+169T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581744 | ||||||
chr2:38582012
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.730-27A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/12 | chr2 | 38582012 | ||||||
chr2:38582020
|
C | T | 103 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(100): Show | 137 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.730-35G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/12 | chr2 | 38582020 | ||||||
chr2:38582297
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.633-129A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582297 | ||||||
chr2:38582388
|
G | A | 3 | a0001c0001t0003g0004a0001c0001t0003g0077a0001c0001t0020g0076 | 9 | HG00609.hp2 HG02155.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.633-220C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582388 | ||||||
chr2:38582403
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0135 | 3 | HG00099.hp2 HG00735.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.633-235G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582403 | ||||||
chr2:38582404
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.633-236C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582404 | ||||||
chr2:38582441
|
G | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633-273C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582441 | ||||||
chr2:38582484
|
A | AT | 5 | a0001c0001t0001g0081a0001c0001t0001g0110a0001c0001t0001g0120others(2): Show | 5 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-317dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582484 | ||||||
chr2:38582526
|
T | C | 20 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(17): Show | 32 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.633-358A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582526 | ||||||
chr2:38582528
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-360A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582528 | ||||||
chr2:38582557
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633-389C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582557 | ||||||
chr2:38582599
|
T | C | 46 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0150others(43): Show | 58 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.633-431A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582599 | ||||||
chr2:38582637
|
T | A | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633-469A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582637 | ||||||
chr2:38582669
|
C | T | 1 | a0002c0002t0006g0255 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.633-501G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582669 | ||||||
chr2:38582717
|
C | G | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0002c0002t0013g0252others(2): Show | 5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-549G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582717 | ||||||
chr2:38582730
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-562C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582730 | ||||||
chr2:38582756
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-588G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582756 | ||||||
chr2:38582779
|
G | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.633-611C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582779 | ||||||
chr2:38582828
|
G | A | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633-660C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582828 | ||||||
chr2:38582830
|
G | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0097 | 4 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-662C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582830 | ||||||
chr2:38582862
|
A | G | 106 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0001g0171others(103): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.633-694T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582862 | ||||||
chr2:38582874
|
T | TA | 8 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-707dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582874 | ||||||
chr2:38582876
|
A | C | 4 | a0001c0001t0010g0029a0001c0001t0010g0233a0001c0001t0010g0238others(1): Show | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-708T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582876 | ||||||
chr2:38582971
|
G | A | 2 | a0001c0001t0016g0102a0001c0001t0016g0109 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.633-803C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582971 | ||||||
chr2:38583022
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.632+819G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583022 | ||||||
chr2:38583152
|
A | AT | 4 | a0001c0001t0010g0029a0001c0001t0010g0233a0001c0001t0010g0238others(1): Show | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+688dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583152 | ||||||
chr2:38583152
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.632+689T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583152 | ||||||
chr2:38583167
|
A | T | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632+674T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583167 | ||||||
chr2:38583298
|
C | A | 4 | a0001c0001t0010g0029a0001c0001t0010g0233a0001c0001t0010g0238others(1): Show | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+543G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583298 | ||||||
chr2:38583338
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.632+503A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583338 | ||||||
chr2:38583485
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.632+356T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583485 | ||||||
chr2:38583679
|
G | A | 41 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.632+162C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583679 | ||||||
chr2:38583786
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0106a0001c0001t0001g0129others(2): Show | 6 | HG01255.hp2 HG03831.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.632+55T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583786 | ||||||
chr2:38584077
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.547-151G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584077 | ||||||
chr2:38584127
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.547-201A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584127 | ||||||
chr2:38584178
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.547-252T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584178 | ||||||
chr2:38584185
|
C | T | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-259G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584185 | ||||||
chr2:38584218
|
C | T | 1 | a0001c0001t0012g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.547-292G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584218 | ||||||
chr2:38584245
|
A | G | 3 | a0001c0001t0007g0099a0001c0001t0007g0152a0001c0001t0007g0168 | 3 | HG02280.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.547-319T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584245 | ||||||
chr2:38584321
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-395T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584321 | ||||||
chr2:38584396
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.547-470G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584396 | ||||||
chr2:38584540
|
T | A | 41 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.547-614A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584540 | ||||||
chr2:38584687
|
A | G | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.547-761T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584687 | ||||||
chr2:38584750
|
C | G | 5 | a0001c0001t0007g0099a0001c0001t0007g0152a0001c0001t0007g0168others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-824G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584750 | ||||||
chr2:38584789
|
T | G | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.546+855A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584789 | ||||||
chr2:38584814
|
TAA | T | 14 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0037others(11): Show | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.546+828_546+829del others(2): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584814 | ||||||
chr2:38584878
|
T | G | 2 | a0001c0001t0010g0238a0001c0001t0010g0241 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.546+766A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584878 | ||||||
chr2:38584971
|
A | G | 2 | a0001c0001t0007g0078a0001c0001t0007g0148 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.546+673T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584971 | ||||||
chr2:38585025
|
T | A | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.546+619A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585025 | ||||||
chr2:38585036
|
C | T | 1 | a0001c0001t0024g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.546+608G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585036 | ||||||
chr2:38585074
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.546+570G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585074 | ||||||
chr2:38585122
|
GTAGGAAG others(5): Show |
G | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.546+510_546+521del others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585122 | ||||||
chr2:38585356
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+288C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585356 | ||||||
chr2:38585376
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0216 | 3 | NA18979.hp1 NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.546+268T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585376 | ||||||
chr2:38585410
|
G | A | 1 | a0001c0001t0016g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.546+234C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585410 | ||||||
chr2:38585514
|
A | G | 21 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0002g0003others(18): Show | 29 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.546+130T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585514 | ||||||
chr2:38585518
|
T | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+126A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585518 | ||||||
chr2:38585538
|
A | G | 2 | a0001c0001t0016g0102a0001c0001t0016g0109 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.546+106T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585538 | ||||||
chr2:38585948
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.309-67A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38585948 | ||||||
chr2:38586015
|
C | G | 18 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(15): Show | 26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-134G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586015 | ||||||
chr2:38586025
|
C | CT | 9 | a0001c0001t0004g0250a0002c0002t0006g0255a0002c0002t0006g0256others(6): Show | 9 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.309-145dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586025 | ||||||
chr2:38586038
|
TTGAGACG others(11): Show |
T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0229 | 3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-175_309-158del others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586038 | ||||||
chr2:38586057
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0229 | 3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-176A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586057 | ||||||
chr2:38586061
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309-180C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586061 | ||||||
chr2:38586061
|
G | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0229 | 3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-180C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586061 | ||||||
chr2:38586062
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-181G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586062 | ||||||
chr2:38586107
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309-226G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586107 | ||||||
chr2:38586240
|
C | G | 1 | a0001c0001t0014g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.309-359G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586240 | ||||||
chr2:38586257
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.309-376C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586257 | ||||||
chr2:38586273
|
G | A | 18 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(15): Show | 26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-392C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586273 | ||||||
chr2:38586299
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.309-418C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586299 | ||||||
chr2:38586430
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.309-549A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586430 | ||||||
chr2:38586477
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0155 | 4 | HG02451.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.309-596C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586477 | ||||||
chr2:38586560
|
G | A | 12 | a0001c0001t0010g0029a0001c0001t0010g0233a0001c0001t0010g0238others(9): Show | 13 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.309-679C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586560 | ||||||
chr2:38586581
|
C | A | 1 | a0001c0001t0022g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.309-700G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586581 | ||||||
chr2:38586605
|
T | C | 16 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(13): Show | 25 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.309-724A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586605 | ||||||
chr2:38586634
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.309-753A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586634 | ||||||
chr2:38586655
|
T | G | 18 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(15): Show | 26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-774A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586655 | ||||||
chr2:38586757
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309-876C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586757 | ||||||
chr2:38586863
|
A | G | 41 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0002g0003others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.309-982T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586863 | ||||||
chr2:38586902
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.309-1021C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586902 | ||||||
chr2:38587049
|
T | C | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0002c0002t0013g0252others(2): Show | 5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-1168A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587049 | ||||||
chr2:38587126
|
T | G | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.309-1245A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587126 | ||||||
chr2:38587177
|
G | A | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309-1296C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587177 | ||||||
chr2:38587284
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.309-1403T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587284 | ||||||
chr2:38587313
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0018g0108 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.309-1432A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587313 | ||||||
chr2:38587365
|
ATTAT | A | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.309-1488_309-1485d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587365 | ||||||
chr2:38587375
|
G | A | 99 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(96): Show | 130 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.309-1494C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587375 | ||||||
chr2:38587380
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.309-1499A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587380 | ||||||
chr2:38587464
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0019g0175 | 5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-1583G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587464 | ||||||
chr2:38587506
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.309-1625C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587506 | ||||||
chr2:38587535
|
C | T | 5 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0243others(2): Show | 7 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-1654G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587535 | ||||||
chr2:38587644
|
G | GA | 21 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 30 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.309-1764dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587644 | ||||||
chr2:38587691
|
T | C | 15 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(12): Show | 22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.309-1810A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587691 | ||||||
chr2:38587712
|
T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309-1831A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587712 | ||||||
chr2:38587813
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.309-1932A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587813 | ||||||
chr2:38587867
|
G | A | 1 | a0001c0001t0017g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.309-1986C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587867 | ||||||
chr2:38587963
|
T | G | 1 | a0001c0001t0002g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.309-2082A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587963 | ||||||
chr2:38587975
|
C | CT | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2095dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587975 | ||||||
chr2:38587999
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2118A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587999 | ||||||
chr2:38588060
|
G | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2179C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588060 | ||||||
chr2:38588100
|
G | A | 1 | a0001c0001t0023g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.309-2219C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588100 | ||||||
chr2:38588107
|
G | A | 34 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(31): Show | 50 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.309-2226C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588107 | ||||||
chr2:38588119
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2238G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588119 | ||||||
chr2:38588142
|
C | T | 1 | a0001c0001t0009g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309-2261G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588142 | ||||||
chr2:38588164
|
T | C | 11 | a0001c0001t0016g0102a0001c0001t0016g0109a0001c0001t0018g0108others(8): Show | 11 | HG02630.hp2 HG02922.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.309-2283A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588164 | ||||||
chr2:38588222
|
T | C | 42 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0170others(39): Show | 53 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.309-2341A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588222 | ||||||
chr2:38588245
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.309-2364C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588245 | ||||||
chr2:38588420
|
G | T | 1 | a0002c0002t0006g0260 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.309-2539C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588420 | ||||||
chr2:38588505
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.309-2624G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588505 | ||||||
chr2:38588542
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(243): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.309-2661T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588542 | ||||||
chr2:38588546
|
C | CA | 15 | a0001c0001t0001g0074a0001c0001t0001g0127a0001c0001t0001g0142others(12): Show | 15 | HG00673.hp1 HG01358.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.309-2666dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAA | 10 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0106others(7): Show | 15 | HG01255.hp2 HG02109.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.309-2667_309-2666d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAA | 5 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.309-2671_309-2666d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA | 17 | a0001c0001t0001g0091a0001c0001t0002g0008a0001c0001t0002g0016others(14): Show | 21 | HG00639.hp1 HG00738.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.309-2672_309-2666d others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(1): Show |
19 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0144others(16): Show | 22 | HG01070.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.309-2673_309-2666d others(10): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(2): Show |
15 | a0001c0001t0002g0031a0001c0001t0002g0069a0001c0001t0002g0239others(12): Show | 23 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.309-2674_309-2666d others(11): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0004g0247a0003c0003t0004g0248a0003c0003t0004g0249 | 3 | NA18940.hp1 NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.309-2675_309-2666d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.309-2677_309-2666d others(14): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0171 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.309-2679_309-2666d others(16): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.309-2680_309-2666d others(17): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.309-2681_309-2666d others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(12): Show |
2 | a0002c0002t0006g0255a0002c0002t0006g0256 | 2 | NA18951.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.309-2684_309-2666d others(21): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(13): Show |
1 | a0002c0002t0006g0257 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.309-2685_309-2666d others(22): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(24): Show |
1 | a0002c0002t0006g0258 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.309-2666_309-2665i others(33): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(25): Show |
2 | a0002c0002t0006g0259a0002c0002t0006g0262 | 2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.309-2666_309-2665i others(34): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
C | CAAAAAAA others(29): Show |
2 | a0002c0002t0006g0260a0002c0002t0006g0261 | 2 | NA18994.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.309-2666_309-2665i others(38): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
CAAAA | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(10): Show | 22 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.309-2669_309-2666d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
CAAAAA | C | 10 | a0001c0001t0007g0078a0001c0001t0007g0099a0001c0001t0007g0148others(7): Show | 11 | HG01496.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.309-2670_309-2666d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588546
|
CAAAAAAA others(3): Show |
C | 24 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(21): Show | 32 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.309-2675_309-2666d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | ||||||
chr2:38588591
|
A | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2710T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588591 | ||||||
chr2:38588726
|
G | GT | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2803dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588726 | ||||||
chr2:38588754
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.308+2776T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588754 | ||||||
chr2:38588835
|
G | C | 1 | a0002c0002t0006g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.308+2695C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588835 | ||||||
chr2:38588876
|
C | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2654G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588876 | ||||||
chr2:38588889
|
C | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2641G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588889 | ||||||
chr2:38588932
|
T | C | 39 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(36): Show | 55 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.308+2598A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588932 | ||||||
chr2:38588993
|
T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+2537A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588993 | ||||||
chr2:38589035
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG01099.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.308+2495T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589035 | ||||||
chr2:38589125
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.308+2405G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589125 | ||||||
chr2:38589219
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2311T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589219 | ||||||
chr2:38589258
|
A | C | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.308+2272T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589258 | ||||||
chr2:38589677
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1853C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589677 | ||||||
chr2:38589766
|
A | C | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1764T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589766 | ||||||
chr2:38589782
|
C | A | 4 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(1): Show | 4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.308+1748G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589782 | ||||||
chr2:38589844
|
T | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1686A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589844 | ||||||
chr2:38589845
|
T | G | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1685A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589845 | ||||||
chr2:38589879
|
T | C | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1651A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589879 | ||||||
chr2:38590070
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1460A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590070 | ||||||
chr2:38590184
|
T | C | 15 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(12): Show | 22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.308+1346A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590184 | ||||||
chr2:38590260
|
C | T | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+1270G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590260 | ||||||
chr2:38590272
|
G | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+1258C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590272 | ||||||
chr2:38590448
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.308+1082A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590448 | ||||||
chr2:38590641
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0019g0175 | 5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+889C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590641 | ||||||
chr2:38590844
|
A | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+686T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590844 | ||||||
chr2:38590862
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+668C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590862 | ||||||
chr2:38590967
|
T | C | 1 | a0001c0001t0007g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.308+563A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590967 | ||||||
chr2:38590986
|
C | CAG | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+542_308+543dup others(2): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590986 | ||||||
chr2:38590997
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308+533G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590997 | ||||||
chr2:38591079
|
C | T | 99 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0170others(96): Show | 129 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.308+451G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591079 | ||||||
chr2:38591108
|
C | T | 41 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0002g0003others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.308+422G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591108 | ||||||
chr2:38591229
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+301G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591229 | ||||||
chr2:38591283
|
T | C | 35 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(32): Show | 51 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.308+247A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591283 | ||||||
chr2:38591352
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0019g0175 | 5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+178C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591352 | ||||||
chr2:38591406
|
T | C | 3 | a0001c0001t0008g0197a0001c0001t0008g0198a0001c0001t0008g0212 | 3 | NA18956.hp1 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.308+124A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591406 | ||||||
chr2:38591459
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.308+71C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591459 | ||||||
chr2:38591503
|
T | G | 2 | a0001c0001t0007g0152a0001c0001t0007g0168 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.308+27A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591503 | ||||||
chr2:38591678
|
A | C | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0250others(4): Show | 12 | HG00423.hp2 NA18940.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-30T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591678 | ||||||
chr2:38591698
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-50C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591698 | ||||||
chr2:38591833
|
A | G | 40 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(37): Show | 51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.190-185T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591833 | ||||||
chr2:38591840
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.190-192C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591840 | ||||||
chr2:38591902
|
G | A | 15 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(12): Show | 22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-254C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591902 | ||||||
chr2:38591907
|
T | C | 2 | a0001c0001t0007g0148a0001c0001t0007g0232 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-259A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591907 | ||||||
chr2:38591951
|
G | A | 1 | a0001c0001t0007g0148 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-303C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591951 | ||||||
chr2:38591972
|
T | A | 1 | a0001c0001t0005g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.190-324A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591972 | ||||||
chr2:38591975
|
C | CA | 5 | a0001c0001t0001g0096a0001c0001t0009g0023a0001c0001t0009g0156others(2): Show | 6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-328dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591975 | ||||||
chr2:38592001
|
T | C | 2 | a0001c0001t0007g0148a0001c0001t0007g0232 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-353A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592001 | ||||||
chr2:38592099
|
A | G | 1 | a0001c0001t0004g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.190-451T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592099 | ||||||
chr2:38592180
|
A | G | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.190-532T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592180 | ||||||
chr2:38592279
|
A | AGTTGTT | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-632_190-631ins others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592279 | ||||||
chr2:38592328
|
C | T | 40 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(37): Show | 51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.190-680G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592328 | ||||||
chr2:38592384
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.190-736C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592384 | ||||||
chr2:38592418
|
G | A | 1 | a0001c0001t0008g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.190-770C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592418 | ||||||
chr2:38592440
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.190-792A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592440 | ||||||
chr2:38592499
|
A | G | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 16 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.190-851T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592499 | ||||||
chr2:38592523
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190-875C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592523 | ||||||
chr2:38592557
|
C | G | 55 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(52): Show | 70 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.190-909G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592557 | ||||||
chr2:38592565
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.190-917G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592565 | ||||||
chr2:38592604
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.190-956C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592604 | ||||||
chr2:38592627
|
T | C | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-979A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592627 | ||||||
chr2:38592636
|
A | G | 1 | a0001c0001t0005g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.190-988T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592636 | ||||||
chr2:38592764
|
G | A | 41 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(38): Show | 52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.190-1116C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592764 | ||||||
chr2:38592765
|
T | C | 4 | a0001c0001t0010g0029a0001c0001t0010g0233a0001c0001t0010g0238others(1): Show | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1117A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592765 | ||||||
chr2:38592801
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.190-1153A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592801 | ||||||
chr2:38592809
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.190-1161T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592809 | ||||||
chr2:38592860
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.190-1212G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592860 | ||||||
chr2:38592958
|
T | C | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-1310A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592958 | ||||||
chr2:38592970
|
A | G | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0239others(1): Show | 6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1322T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592970 | ||||||
chr2:38593036
|
T | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(10): Show | 21 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-1388A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593036 | ||||||
chr2:38593289
|
T | C | 38 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(35): Show | 54 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.190-1641A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593289 | ||||||
chr2:38593295
|
T | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1647A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593295 | ||||||
chr2:38593380
|
T | C | 67 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0170others(64): Show | 82 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-1732A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593380 | ||||||
chr2:38593393
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG00597.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.190-1745A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593393 | ||||||
chr2:38593414
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1766A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593414 | ||||||
chr2:38593420
|
G | C | 5 | a0001c0001t0002g0166a0001c0001t0002g0167a0002c0002t0013g0252others(2): Show | 5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1772C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593420 | ||||||
chr2:38593536
|
A | G | 1 | a0001c0001t0023g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.190-1888T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593536 | ||||||
chr2:38593603
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1955A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593603 | ||||||
chr2:38593800
|
C | T | 21 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 29 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.190-2152G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593800 | ||||||
chr2:38593858
|
G | A | 1 | a0001c0001t0007g0148 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-2210C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593858 | ||||||
chr2:38593862
|
C | CA | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(180): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.190-2215dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | ||||||
chr2:38593862
|
C | CAA | 13 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(10): Show | 21 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-2216_190-2215d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | ||||||
chr2:38593862
|
C | CAAA | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2217_190-2215d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | ||||||
chr2:38593873
|
C | A | 9 | a0001c0001t0001g0150a0002c0002t0006g0255a0002c0002t0006g0256others(6): Show | 9 | HG02056.hp1 NA18945.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-2225G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593873 | ||||||
chr2:38593881
|
A | C | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-2233T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593881 | ||||||
chr2:38593882
|
A | C | 1 | a0001c0001t0012g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.190-2234T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593882 | ||||||
chr2:38594031
|
C | T | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.190-2383G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594031 | ||||||
chr2:38594082
|
G | A | 1 | a0001c0001t0002g0060 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.190-2434C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594082 | ||||||
chr2:38594174
|
C | CA | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0221others(2): Show | 5 | HG02074.hp1 HG02273.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-2527dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594174 | ||||||
chr2:38594192
|
CA | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2545delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594192 | ||||||
chr2:38594199
|
C | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2551G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594199 | ||||||
chr2:38594210
|
A | C | 15 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(12): Show | 19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-2562T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594210 | ||||||
chr2:38594332
|
A | G | 1 | a0001c0001t0003g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.190-2684T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594332 | ||||||
chr2:38594371
|
G | A | 117 | a0001c0001t0001g0047a0001c0001t0001g0091a0001c0001t0001g0092others(114): Show | 150 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.190-2723C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594371 | ||||||
chr2:38594423
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.190-2775C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594423 | ||||||
chr2:38594477
|
A | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0097a0001c0001t0007g0099others(1): Show | 6 | HG02280.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-2829T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594477 | ||||||
chr2:38594550
|
A | G | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.190-2902T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594550 | ||||||
chr2:38594569
|
G | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2921C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594569 | ||||||
chr2:38594747
|
C | T | 8 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0039others(5): Show | 10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-3099G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594747 | ||||||
chr2:38594755
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(259): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.190-3107T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594755 | ||||||
chr2:38594795
|
G | C | 9 | a0001c0001t0007g0099a0002c0002t0006g0255a0002c0002t0006g0256others(6): Show | 9 | HG02280.hp1 NA18945.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-3147C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594795 | ||||||
chr2:38594853
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.190-3205T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594853 | ||||||
chr2:38594871
|
T | C | 1 | a0001c0001t0012g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.190-3223A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594871 | ||||||
chr2:38594871
|
T | G | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-3223A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594871 | ||||||
chr2:38594933
|
C | A | 14 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.190-3285G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594933 | ||||||
chr2:38595014
|
T | C | 21 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(18): Show | 29 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.190-3366A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595014 | ||||||
chr2:38595107
|
C | T | 1 | a0001c0001t0007g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-3459G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595107 | ||||||
chr2:38595250
|
G | A | 1 | a0003c0003t0004g0249 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.190-3602C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595250 | ||||||
chr2:38595272
|
T | TA | 29 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0135others(26): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.190-3625dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595272
|
TA | T | 17 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0104others(14): Show | 17 | HG00323.hp1 HG00323.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-3625delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595272
|
TAA | T | 34 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0002g0030others(31): Show | 46 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.190-3626_190-3625d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595272
|
TAAA | T | 39 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0002g0003others(36): Show | 50 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.190-3627_190-3625d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595272
|
TAAAAAA | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-3630_190-3625d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595272
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0021g0242 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.190-3634_190-3625d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | ||||||
chr2:38595276
|
A | T | 1 | a0001c0001t0024g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190-3628T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595276 | ||||||
chr2:38595292
|
A | G | 15 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(12): Show | 19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-3644T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595292 | ||||||
chr2:38595293
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18970.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.190-3645T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595293 | ||||||
chr2:38595294
|
A | G | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-3646T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595294 | ||||||
chr2:38595308
|
A | C | 2 | a0001c0001t0002g0040a0001c0001t0005g0039 | 2 | HG01169.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.190-3660T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595308 | ||||||
chr2:38595310
|
A | ACAC | 38 | a0001c0001t0001g0047a0001c0001t0001g0170a0001c0001t0002g0003others(35): Show | 49 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.190-3665_190-3663d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595310 | ||||||
chr2:38595310
|
A | C | 2 | a0001c0001t0002g0040a0001c0001t0005g0039 | 2 | HG01169.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.190-3662T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595310 | ||||||
chr2:38595370
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.190-3722A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595370 | ||||||
chr2:38595582
|
C | T | 1 | a0001c0001t0007g0148 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-3934G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595582 | ||||||
chr2:38595583
|
G | A | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-3935C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595583 | ||||||
chr2:38595613
|
G | C | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-3965C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595613 | ||||||
chr2:38595700
|
C | T | 3 | a0001c0001t0011g0028a0001c0001t0011g0222a0001c0001t0011g0223 | 4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-4052G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595700 | ||||||
chr2:38595701
|
G | A | 14 | a0001c0001t0002g0095a0001c0001t0004g0032a0001c0001t0004g0033others(11): Show | 21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.190-4053C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595701 | ||||||
chr2:38595713
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4065C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595713 | ||||||
chr2:38595776
|
A | G | 44 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0150others(41): Show | 55 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.190-4128T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595776 | ||||||
chr2:38595812
|
C | G | 1 | a0001c0001t0007g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-4164G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595812 | ||||||
chr2:38595839
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4191C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595839 | ||||||
chr2:38595843
|
C | CA | 13 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0243others(10): Show | 20 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.190-4196dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595843 | ||||||
chr2:38595939
|
C | A | 11 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(8): Show | 19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.190-4291G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595939 | ||||||
chr2:38595988
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.190-4340C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595988 | ||||||
chr2:38595993
|
T | C | 11 | a0001c0001t0002g0095a0001c0001t0003g0004a0001c0001t0003g0017others(8): Show | 19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.190-4345A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595993 | ||||||
chr2:38596069
|
TA | T | 12 | a0001c0001t0001g0098a0002c0002t0006g0255a0002c0002t0006g0256others(9): Show | 12 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-4422delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596069 | ||||||
chr2:38596236
|
G | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-4588C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596236 | ||||||
chr2:38596342
|
C | CCT | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(249): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.190-4696_190-4695d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596342 | ||||||
chr2:38596434
|
G | GT | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-4787dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596434 | ||||||
chr2:38596463
|
T | G | 24 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0243others(21): Show | 31 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.190-4815A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596463 | ||||||
chr2:38596481
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4833A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596481 | ||||||
chr2:38596482
|
T | G | 3 | a0001c0001t0007g0078a0001c0001t0007g0148a0001c0001t0007g0232 | 3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-4834A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596482 | ||||||
chr2:38596526
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190-4878C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596526 | ||||||
chr2:38596527
|
G | C | 1 | a0001c0001t0022g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-4879C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596527 | ||||||
chr2:38596540
|
G | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0063 | 2 | HG00673.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.190-4892C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596540 | ||||||
chr2:38596712
|
T | C | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.190-5064A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596712 | ||||||
chr2:38596735
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-5087C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596735 | ||||||
chr2:38596800
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190-5152G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596800 | ||||||
chr2:38596856
|
C | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-5208G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596856 | ||||||
chr2:38597145
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+5293A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597145 | ||||||
chr2:38597233
|
A | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+5205T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597233 | ||||||
chr2:38597268
|
T | C | 1 | a0001c0001t0012g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.189+5170A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597268 | ||||||
chr2:38597287
|
C | G | 1 | a0001c0001t0002g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189+5151G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597287 | ||||||
chr2:38597386
|
CAAGAAT | C | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+5046_189+5051d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597386 | ||||||
chr2:38597501
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.189+4937G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597501 | ||||||
chr2:38597578
|
A | G | 1 | a0001c0001t0004g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189+4860T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597578 | ||||||
chr2:38597584
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4854T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597584 | ||||||
chr2:38597632
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0216 | 5 | NA18979.hp1 NA19009.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4806C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597632 | ||||||
chr2:38597639
|
T | A | 43 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0150others(40): Show | 54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+4799A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597639 | ||||||
chr2:38597671
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+4767A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597671 | ||||||
chr2:38597680
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.189+4758A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597680 | ||||||
chr2:38597683
|
C | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+4755G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597683 | ||||||
chr2:38597691
|
A | AT | 22 | a0001c0001t0002g0036a0001c0001t0002g0097a0001c0001t0004g0032others(19): Show | 29 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.189+4746dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597691 | ||||||
chr2:38597691
|
AT | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0025others(65): Show | 87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.189+4746delA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597691 | ||||||
chr2:38597693
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0155 | 4 | HG02451.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4745A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597693 | ||||||
chr2:38597697
|
T | A | 4 | a0001c0001t0009g0023a0001c0001t0009g0156a0001c0001t0009g0157others(1): Show | 5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4741A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597697 | ||||||
chr2:38597751
|
C | T | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4687G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597751 | ||||||
chr2:38597771
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189+4667G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597771 | ||||||
chr2:38597835
|
G | A | 11 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(8): Show | 14 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4603C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597835 | ||||||
chr2:38597950
|
T | C | 1 | a0001c0001t0008g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189+4488A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597950 | ||||||
chr2:38597966
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+4472G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597966 | ||||||
chr2:38597983
|
G | A | 42 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(39): Show | 53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4455C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597983 | ||||||
chr2:38598057
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG01106.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.189+4381G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598057 | ||||||
chr2:38598079
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4359A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598079 | ||||||
chr2:38598101
|
AAAAAC | A | 42 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(39): Show | 53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4332_189+4336d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598101 | ||||||
chr2:38598211
|
G | A | 10 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0018others(7): Show | 18 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.189+4227C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598211 | ||||||
chr2:38598256
|
T | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 14 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4182A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598256 | ||||||
chr2:38598265
|
G | C | 42 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(39): Show | 53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4173C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598265 | ||||||
chr2:38598267
|
G | A | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+4171C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598267 | ||||||
chr2:38598543
|
A | T | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+3895T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598543 | ||||||
chr2:38598557
|
G | A | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3881C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598557 | ||||||
chr2:38598558
|
A | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3880T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598558 | ||||||
chr2:38598582
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.189+3856C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598582 | ||||||
chr2:38598639
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+3799A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598639 | ||||||
chr2:38598874
|
G | A | 1 | a0001c0001t0024g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189+3564C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598874 | ||||||
chr2:38598902
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189+3536T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598902 | ||||||
chr2:38598972
|
G | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+3466C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598972 | ||||||
chr2:38599005
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189+3433C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599005 | ||||||
chr2:38599049
|
C | G | 1 | a0001c0001t0004g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.189+3389G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599049 | ||||||
chr2:38599049
|
C | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3389G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599049 | ||||||
chr2:38599063
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.189+3375T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599063 | ||||||
chr2:38599087
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189+3351A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599087 | ||||||
chr2:38599444
|
G | A | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+2994C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599444 | ||||||
chr2:38599557
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+2881G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599557 | ||||||
chr2:38599561
|
A | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+2877T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599561 | ||||||
chr2:38599611
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+2827C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599611 | ||||||
chr2:38599695
|
C | T | 1 | a0001c0001t0014g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.189+2743G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599695 | ||||||
chr2:38599731
|
CTA | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG00639.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.189+2705_189+2706d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599731 | ||||||
chr2:38599753
|
C | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+2685G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599753 | ||||||
chr2:38599758
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.189+2680G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599758 | ||||||
chr2:38599783
|
T | C | 15 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(12): Show | 19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+2655A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599783 | ||||||
chr2:38599928
|
G | A | 1 | a0001c0001t0019g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+2510C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599928 | ||||||
chr2:38600009
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+2429C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600009 | ||||||
chr2:38600019
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189+2419T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600019 | ||||||
chr2:38600124
|
T | G | 1 | a0001c0001t0007g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189+2314A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600124 | ||||||
chr2:38600217
|
C | G | 1 | a0001c0001t0022g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.189+2221G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600217 | ||||||
chr2:38600242
|
A | G | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+2196T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600242 | ||||||
chr2:38600292
|
C | A | 1 | a0001c0001t0004g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.189+2146G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600292 | ||||||
chr2:38600292
|
CG | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0025others(59): Show | 80 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+2145delC | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600292 | ||||||
chr2:38600315
|
A | G | 14 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0017others(11): Show | 25 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.189+2123T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600315 | ||||||
chr2:38600637
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189+1801C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600637 | ||||||
chr2:38600648
|
G | A | 1 | a0001c0001t0004g0033 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.189+1790C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600648 | ||||||
chr2:38600687
|
C | T | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1751G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600687 | ||||||
chr2:38600749
|
C | CA | 18 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(15): Show | 18 | HG00140.hp1 HG01099.hp1 HG03139.hp2 others(15): Show |
intron_variant | MODIFIER | c.189+1688dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600749 | ||||||
chr2:38600749
|
CA | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0176others(3): Show | 6 | HG01081.hp2 HG02145.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1688delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600749 | ||||||
chr2:38600768
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.189+1670A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600768 | ||||||
chr2:38600770
|
T | C | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+1668A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600770 | ||||||
chr2:38600811
|
T | C | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1627A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600811 | ||||||
chr2:38600823
|
C | G | 43 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0002g0003others(40): Show | 54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+1615G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600823 | ||||||
chr2:38600884
|
A | C | 4 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(1): Show | 4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1554T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600884 | ||||||
chr2:38601115
|
C | CG | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1322_189+1323i others(3): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601115 | ||||||
chr2:38601189
|
A | G | 2 | a0001c0001t0007g0078a0001c0001t0007g0232 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.189+1249T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601189 | ||||||
chr2:38601229
|
T | C | 11 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(8): Show | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1209A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601229 | ||||||
chr2:38601362
|
T | A | 7 | a0001c0001t0002g0016a0001c0001t0002g0065a0001c0001t0002g0066others(4): Show | 8 | HG02280.hp2 HG02559.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.189+1076A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601362 | ||||||
chr2:38601375
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0003g0077a0001c0001t0020g0076 | 9 | HG00609.hp2 HG02155.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+1063T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601375 | ||||||
chr2:38601396
|
G | A | 42 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0014others(39): Show | 53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+1042C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601396 | ||||||
chr2:38601464
|
A | G | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+974T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601464 | ||||||
chr2:38601561
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189+877T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601561 | ||||||
chr2:38601581
|
G | A | 1 | a0001c0001t0019g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+857C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601581 | ||||||
chr2:38601654
|
G | A | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+784C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601654 | ||||||
chr2:38601677
|
T | C | 1 | a0001c0001t0010g0241 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189+761A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601677 | ||||||
chr2:38601695
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0025others(59): Show | 80 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+743C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601695 | ||||||
chr2:38601719
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.189+719T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601719 | ||||||
chr2:38601719
|
A | T | 4 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(1): Show | 4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+719T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601719 | ||||||
chr2:38601809
|
G | C | 15 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(12): Show | 19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+629C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601809 | ||||||
chr2:38601815
|
G | T | 1 | a0001c0001t0010g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.189+623C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601815 | ||||||
chr2:38601859
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+579C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601859 | ||||||
chr2:38601897
|
T | G | 2 | a0001c0001t0001g0224a0001c0001t0004g0251 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.189+541A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601897 | ||||||
chr2:38602028
|
G | A | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(4): Show | 7 | HG01106.hp1 HG01175.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+410C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602028 | ||||||
chr2:38602061
|
G | A | 8 | a0002c0002t0006g0255a0002c0002t0006g0256a0002c0002t0006g0257others(5): Show | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+377C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602061 | ||||||
chr2:38602132
|
C | G | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+306G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602132 | ||||||
chr2:38602139
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0002g0072 | 3 | HG00423.hp1 NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.189+299G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602139 | ||||||
chr2:38602148
|
G | T | 3 | a0002c0002t0013g0252a0002c0002t0013g0253a0002c0002t0013g0254 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+290C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602148 | ||||||
chr2:38602253
|
C | T | 43 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0002g0003others(40): Show | 54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+185G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602253 | ||||||
chr2:38602268
|
G | A | 1 | a0001c0001t0007g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+170C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602268 | ||||||
chr2:38602346
|
G | C | 12 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0234others(9): Show | 15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+92C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602346 | ||||||
chr2:38602420
|
G | A | 13 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0243others(10): Show | 20 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+18C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602420 |