Item | Value |
---|---|
geneid | 9581 |
ensemblid | ENSG00000138078.16 |
hgncid | 30228 |
symbol | PREPL |
name | prolyl endopeptidase like |
refseq_nuc | NM_001171613.2 |
refseq_prot | NP_001165084.1 |
ensembl_nuc | ENST00000409411.6 |
ensembl_prot | ENSP00000387095.2 |
mane_status | MANE Select |
chr | chr2 |
start | 44317607 |
end | 44361494 |
strand | - |
ver | v1.2 |
region | chr2:44317607-44361494 |
region5000 | chr2:44312607-44366494 |
regionname0 | PREPL_chr2_44317607_44361494 |
regionname5000 | PREPL_chr2_44312607_44366494 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 638 | 368 | 85 | 67 | 166 | 10 | 38 | 132 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0002 | 0/0 | 638 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0003 | 0/0 | 638 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0004 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0005 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0006 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0007 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0008 | 0/0 | 638 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0009 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0010 | 0/0 | 638 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
a0011 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | MDAFE others(633): Show |
chr2 | 44312607 | 44366494 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1914 | 352 | 72 | 64 | 166 | 10 | 38 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0001c0002 | 0/0 | 1914 | 14 | 12 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0001c0008 | 0/0 | 1914 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0001c0010 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0002c0003 | 0/0 | 1914 | 4 | 4 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0003c0004 | 0/0 | 1914 | 2 | 1 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0004c0012 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0005c0005 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0006c0011 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0007c0014 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0008c0006 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0009c0009 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0010c0007 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 | ||
a0011c0013 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | ATGGA others(1909): Show |
chr2 | 44312607 | 44366494 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5829 | 92 | 4 | 13 | 69 | 0 | 5 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0002 | 0/0 | 5829 | 87 | 3 | 26 | 38 | 6 | 14 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0003 | 0/0 | 5829 | 20 | 16 | 4 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0004 | 0/0 | 5825 | 22 | 0 | 0 | 20 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5820): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0005 | 0/0 | 5829 | 20 | 2 | 3 | 2 | 0 | 13 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0006 | 0/0 | 5826 | 9 | 8 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5821): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0007 | 0/0 | 5827 | 10 | 10 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0008 | 0/0 | 5829 | 9 | 0 | 0 | 9 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0009 | 0/0 | 5829 | 6 | 1 | 4 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0010 | 0/0 | 5829 | 8 | 0 | 0 | 8 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0011 | 0/0 | 5829 | 7 | 0 | 0 | 7 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0012 | 0/0 | 5827 | 6 | 5 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0013 | 0/0 | 5829 | 4 | 4 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0014 | 0/0 | 5829 | 4 | 2 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0016 | 0/0 | 5829 | 3 | 1 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0018 | 0/0 | 5829 | 3 | 3 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0019 | 0/0 | 5829 | 3 | 0 | 0 | 3 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0021 | 0/0 | 5829 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0022 | 0/0 | 5829 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0023 | 0/0 | 5829 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0024 | 0/0 | 5829 | 2 | 1 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0025 | 0/0 | 5829 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0026 | 0/0 | 5827 | 2 | 0 | 0 | 0 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0027 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0028 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0029 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0030 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0031 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0034 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0035 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0036 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0038 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0039 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0040 | 0/0 | 5827 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0041 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5783): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0042 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0043 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0044 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0046 | 0/0 | 5825 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5820): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0047 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0048 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0049 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0050 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0051 | 0/0 | 5827 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0052 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0053 | 0/1 | 5825 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5820): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0054 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0055 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0057 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0001t0058 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGC others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0002t0003 | 0/0 | 5829 | 7 | 5 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0002t0015 | 0/0 | 5829 | 4 | 4 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0002t0017 | 0/0 | 5827 | 3 | 3 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0001c0008t0001 | 0/0 | 5829 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0001c0010t0037 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0002c0003t0020 | 0/0 | 5827 | 3 | 3 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5822): Show |
chr2 | 44312607 | 44366494 |
a0002c0003t0033 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0003c0004t0009 | 0/0 | 5829 | 2 | 1 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0004c0012t0032 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0005c0005t0003 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0006c0011t0006 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5821): Show |
chr2 | 44312607 | 44366494 |
a0007c0014t0045 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0008c0006t0002 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0009c0009t0013 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0010c0007t0002 | 0/0 | 5829 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
a0011c0013t0056 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | GCAGA others(5824): Show |
chr2 | 44312607 | 44366494 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0001 | 0/0 | 18 | 0 | 11 | 5 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0008g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0009g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0009g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0010g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0010g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0010g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0011g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0011g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0012g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0012g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0012g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0013g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0014g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0014g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0016g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0016g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0018g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0018g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0019g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0019g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0021g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0021g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0022g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0022g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0023g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0023g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0024g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0025g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0026g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0026g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0027g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0028g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0029g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0030g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0031g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0034g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0035g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0036g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0038g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0039g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0040g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0041g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0042g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0043g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0044g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0046g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0047g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0048g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0049g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0050g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0051g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0052g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0053g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0054g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0055g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0057g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0001t0058g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0015g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0015g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0017g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0002t0017g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0008t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0001c0010t0037g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0002c0003t0020g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0002c0003t0020g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0002c0003t0020g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0002c0003t0033g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0003c0004t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0003c0004t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0004c0012t0032g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0005c0005t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0006c0011t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0007c0014t0045g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0008c0006t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0009c0009t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0010c0007t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
a0011c0013t0056g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | GBR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | GBR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | FIN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00280 | hp2 | a0001 | c0001 | t0009 | g0084 | EUR | FIN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00323 | hp2 | a0001 | c0001 | t0029 | g0121 | EUR | FIN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00408 | hp2 | a0001 | c0001 | t0058 | g0292 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00544 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0259 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0155 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00735 | hp1 | a0001 | c0008 | t0001 | g0118 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00738 | hp2 | a0003 | c0004 | t0009 | g0163 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01070 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01070 | hp2 | a0001 | c0001 | t0025 | g0035 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01071 | hp1 | a0001 | c0001 | t0025 | g0035 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01074 | hp2 | a0001 | c0001 | t0014 | g0022 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0156 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01099 | hp2 | a0001 | c0001 | t0014 | g0022 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0282 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01168 | hp1 | a0001 | c0001 | t0052 | g0181 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01168 | hp2 | a0001 | c0001 | t0016 | g0206 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01169 | hp1 | a0001 | c0001 | t0016 | g0030 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01243 | hp2 | a0001 | c0001 | t0050 | g0229 | AMR | PUR | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01256 | hp1 | a0001 | c0001 | t0009 | g0017 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0017 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01261 | hp2 | a0001 | c0001 | t0049 | g0214 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0083 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01496 | hp1 | a0001 | c0001 | t0036 | g0260 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01496 | hp2 | a0001 | c0001 | t0027 | g0047 | AMR | CLM | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01516 | hp2 | a0001 | c0001 | t0030 | g0140 | EUR | IBS | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0081 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01884 | hp2 | a0004 | c0012 | t0032 | g0276 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01943 | hp1 | a0001 | c0001 | t0031 | g0061 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02055 | hp1 | a0001 | c0001 | t0054 | g0231 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02055 | hp2 | a0001 | c0001 | t0013 | g0076 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02145 | hp1 | a0001 | c0001 | t0024 | g0193 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02145 | hp2 | a0001 | c0001 | t0041 | g0281 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02155 | hp2 | a0001 | c0001 | t0011 | g0103 | EAS | CDX | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02257 | hp2 | a0001 | c0001 | t0022 | g0283 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0085 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0279 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02523 | hp1 | a0001 | c0001 | t0024 | g0188 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02523 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | KHV | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02572 | hp2 | a0001 | c0001 | t0022 | g0171 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0256 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02630 | hp1 | a0005 | c0005 | t0003 | g0166 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0042 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02647 | hp2 | a0001 | c0002 | t0015 | g0164 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02717 | hp2 | a0001 | c0001 | t0051 | g0216 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02886 | hp1 | a0006 | c0011 | t0006 | g0058 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02886 | hp2 | a0001 | c0001 | t0057 | g0287 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02895 | hp1 | a0001 | c0001 | t0014 | g0120 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02896 | hp1 | a0002 | c0003 | t0020 | g0290 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02897 | hp1 | a0002 | c0003 | t0020 | g0289 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02922 | hp2 | a0002 | c0003 | t0033 | g0275 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02965 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02965 | hp2 | a0001 | c0001 | t0043 | g0162 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0191 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02976 | hp1 | a0002 | c0003 | t0020 | g0291 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0113 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03041 | hp2 | a0001 | c0001 | t0038 | g0274 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03130 | hp2 | a0001 | c0002 | t0017 | g0271 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03139 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0079 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03195 | hp1 | a0007 | c0014 | t0045 | g0243 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0165 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03209 | hp2 | a0001 | c0001 | t0042 | g0066 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0244 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03239 | hp1 | a0001 | c0001 | t0048 | g0195 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03239 | hp2 | a0008 | c0006 | t0002 | g0263 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0031 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03486 | hp1 | a0001 | c0002 | t0017 | g0272 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0031 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03516 | hp1 | a0001 | c0002 | t0017 | g0075 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | ESN | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03540 | hp2 | a0009 | c0009 | t0013 | g0192 | AFR | GWD | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03579 | hp2 | a0001 | c0001 | t0018 | g0273 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0258 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0190 | SAS | PJL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0182 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0253 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0265 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03942 | hp1 | a0001 | c0001 | t0035 | g0207 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04115 | hp1 | a0001 | c0001 | t0026 | g0235 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04199 | hp1 | a0001 | c0001 | t0026 | g0234 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG04228 | hp2 | a0010 | c0007 | t0002 | g0142 | SAS | STU | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0280 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0169 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18939 | hp1 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18943 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18953 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18961 | hp1 | a0001 | c0001 | t0011 | g0093 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18962 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18965 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18968 | hp1 | a0001 | c0001 | t0021 | g0130 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18969 | hp1 | a0001 | c0001 | t0010 | g0285 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18972 | hp1 | a0001 | c0001 | t0023 | g0249 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18975 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18979 | hp1 | a0001 | c0001 | t0021 | g0131 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18980 | hp2 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18981 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18983 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18984 | hp2 | a0001 | c0001 | t0010 | g0044 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18989 | hp1 | a0001 | c0001 | t0010 | g0284 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18989 | hp2 | a0001 | c0001 | t0047 | g0209 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18994 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18999 | hp1 | a0001 | c0001 | t0019 | g0029 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0087 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19030 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19057 | hp2 | a0001 | c0001 | t0019 | g0180 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19060 | hp2 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19062 | hp1 | a0001 | c0001 | t0039 | g0251 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19064 | hp1 | a0001 | c0001 | t0046 | g0187 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0044 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19080 | hp1 | a0001 | c0001 | t0019 | g0029 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19080 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19088 | hp2 | a0001 | c0001 | t0034 | g0223 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19090 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0157 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA19240 | hp2 | a0001 | c0001 | t0016 | g0030 | AFR | YRI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20129 | hp1 | a0003 | c0004 | t0009 | g0160 | AFR | ASW | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20129 | hp2 | a0001 | c0001 | t0055 | g0286 | AFR | ASW | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20805 | hp1 | a0001 | c0001 | t0044 | g0143 | EUR | TSI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | TSI | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0255 | SAS | GIH | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0277 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | MSL | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0042 | AFR | USA | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
HG06807 | hp2 | a0001 | c0010 | t0037 | g0151 | AFR | USA | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18955 | hp1 | a0001 | c0001 | t0023 | g0254 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20300 | hp1 | a0011 | c0013 | t0056 | g0288 | AFR | USA | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0267 | AFR | USA | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA21309 | hp1 | a0001 | c0001 | t0028 | g0056 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
NA21309 | hp2 | a0001 | c0001 | t0040 | g0150 | AFR | LWK | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
homoSapiens | chm13v2 | a0001 | c0001 | t0053 | g0172 | REF | REF | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | PREPL_chr2_44312607_44366494 | PREPL | chr2 | 44312607 | 44366494 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44321418 | C | T | 2 | a0004 a0009 |
2 | HG01884.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.1855G>A | p.Glu619Lys | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2018/5829 | 1855/1917 | 619/638 | chr2 | 44321418 | |||
chr2:44321429 | T | C | 1 | a0011 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1844A>G | p.Lys615Arg | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2007/5829 | 1844/1917 | 615/638 | chr2 | 44321429 | |||
chr2:44322793 | A | G | 1 | a0010 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1691T>C | p.Ile564Thr | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/14 | 1854/5829 | 1691/1917 | 564/638 | chr2 | 44322793 | |||
chr2:44323296 | T | C | 1 | a0003 | 2 | HG00738.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1595A>G | p.Lys532Arg | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/14 | 1758/5829 | 1595/1917 | 532/638 | chr2 | 44323296 | |||
chr2:44323349 | T | G | 1 | a0006 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1542A>C | p.Glu514Asp | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/14 | 1705/5829 | 1542/1917 | 514/638 | chr2 | 44323349 | |||
chr2:44323389 | T | C | 4 | a0002 a0004 a0007 others(1): Show |
7 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/14 | 1665/5829 | 1502/1917 | 501/638 | chr2 | 44323389 | |||
chr2:44332578 | T | C | 1 | a0007 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.967A>G | p.Ile323Val | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/14 | 1130/5829 | 967/1917 | 323/638 | chr2 | 44332578 | |||
chr2:44332605 | T | A | 1 | a0005 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.940A>T | p.Asn314Tyr | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/14 | 1103/5829 | 940/1917 | 314/638 | chr2 | 44332605 | |||
chr2:44343791 | G | T | 1 | a0008 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.303C>A | p.Ser101Arg | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/14 | 466/5829 | 303/1917 | 101/638 | chr2 | 44343791 | |||
chr2:44361381 | C | T | 2 | a0001 a0006 |
11 | HG01106.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
splice_region_variant | LOW | c.-50G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | chr2 | 44361381 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44321863 | A | G | 1 | a0001c0008 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1791T>C | p.Pro597Pro | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 13/14 | 1954/5829 | 1791/1917 | 597/638 | chr2 | 44321863 | |||
chr2:44322828 | T | C | 2 | a0001c0010 a0003c0004 |
3 | HG00738.hp2 HG06807.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.1656A>G | p.Ala552Ala | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/14 | 1819/5829 | 1656/1917 | 552/638 | chr2 | 44322828 | |||
chr2:44339162 | T | C | 1 | a0003c0004 | 2 | HG00738.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.687A>G | p.Glu229Glu | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/14 | 850/5829 | 687/1917 | 229/638 | chr2 | 44339162 | |||
chr2:44343869 | A | T | 2 | a0001c0002 a0005c0005 |
15 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(12): Show |
synonymous_variant | LOW | c.225T>A | p.Ala75Ala | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/14 | 388/5829 | 225/1917 | 75/638 | chr2 | 44343869 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44317646 | T | A | 1 | a0001c0001t0018 | 3 | HG02647.hp1 HG03579.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3710A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3710 | chr2 | 44317646 | ||||||
chr2:44317667 | TATTTTCA others(34): Show |
T | 1 | a0001c0001t0041 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3648_*3688delTTGA others(37): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3648 | chr2 | 44317667 | ||||||
chr2:44317775 | A | C | 3 | a0001c0001t0004 a0001c0001t0024 a0001c0001t0046 |
25 | HG00597.hp1 HG02056.hp1 HG02071.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3581T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3581 | chr2 | 44317775 | ||||||
chr2:44317797 | C | T | 1 | a0001c0001t0029 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3559G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3559 | chr2 | 44317797 | ||||||
chr2:44317810 | G | A | 4 | a0002c0003t0020 a0002c0003t0033 a0004c0012t0032 others(1): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3546C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3546 | chr2 | 44317810 | ||||||
chr2:44317816 | G | A | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3540C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3540 | chr2 | 44317816 | ||||||
chr2:44317953 | G | C | 1 | a0001c0001t0021 | 2 | NA18968.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3403C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3403 | chr2 | 44317953 | ||||||
chr2:44317959 | AAAT | A | 2 | a0001c0001t0006 a0006c0011t0006 |
10 | HG01106.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3394_*3396delATT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3394 | chr2 | 44317959 | ||||||
chr2:44317973 | T | G | 2 | a0001c0001t0013 a0009c0009t0013 |
5 | HG02055.hp2 HG02970.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3383A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3383 | chr2 | 44317973 | ||||||
chr2:44317987 | T | C | 1 | a0001c0001t0008 | 9 | NA18939.hp1 NA18953.hp2 NA18962.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3369A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3369 | chr2 | 44317987 | ||||||
chr2:44318093 | CTG | C | 3 | a0001c0001t0007 a0001c0001t0012 a0002c0003t0020 |
19 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3261_*3262delCA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3261 | chr2 | 44318093 | ||||||
chr2:44318095 | G | GT | 3 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0039 |
9 | HG02004.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3260dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3260 | chr2 | 44318095 | ||||||
chr2:44318095 | GT | G | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*3260delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3260 | chr2 | 44318095 | ||||||
chr2:44318095 | GTT | G | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0003 others(7): Show |
28 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3260delAA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3259 | chr2 | 44318095 | ||||||
chr2:44318095 | GTTT | G | 6 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0038 others(3): Show |
12 | HG00280.hp2 HG00738.hp2 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3258_*3260delAAA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3258 | chr2 | 44318095 | ||||||
chr2:44318159 | C | T | 4 | a0001c0001t0009 a0001c0001t0038 a0001c0010t0037 others(1): Show |
10 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3197G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3197 | chr2 | 44318159 | ||||||
chr2:44318252 | G | A | 4 | a0002c0003t0020 a0002c0003t0033 a0004c0012t0032 others(1): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3104C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3104 | chr2 | 44318252 | ||||||
chr2:44318282 | G | A | 1 | a0001c0001t0050 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3074C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3074 | chr2 | 44318282 | ||||||
chr2:44318312 | G | C | 1 | a0001c0001t0014 | 4 | HG01074.hp2 HG01099.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3044C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3044 | chr2 | 44318312 | ||||||
chr2:44318345 | C | A | 1 | a0001c0001t0043 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3011G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3011 | chr2 | 44318345 | ||||||
chr2:44318356 | G | C | 1 | a0001c0001t0019 | 3 | NA18999.hp1 NA19057.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3000C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 3000 | chr2 | 44318356 | ||||||
chr2:44318403 | T | G | 1 | a0007c0014t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2953 | chr2 | 44318403 | ||||||
chr2:44318406 | T | G | 3 | a0001c0001t0012 a0001c0001t0022 a0001c0001t0041 |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2950A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2950 | chr2 | 44318406 | ||||||
chr2:44318437 | T | C | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2919A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2919 | chr2 | 44318437 | ||||||
chr2:44318566 | C | G | 1 | a0001c0001t0029 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2790G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2790 | chr2 | 44318566 | ||||||
chr2:44318573 | T | G | 1 | a0001c0001t0026 | 2 | HG04115.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2783A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2783 | chr2 | 44318573 | ||||||
chr2:44318596 | A | ATG | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2759_*2760insCA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2759 | chr2 | 44318596 | ||||||
chr2:44318598 | A | T | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2758T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2758 | chr2 | 44318598 | ||||||
chr2:44318601 | A | C | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2755T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2755 | chr2 | 44318601 | ||||||
chr2:44318601 | A | T | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2755T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2755 | chr2 | 44318601 | ||||||
chr2:44318602 | A | T | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2754T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2754 | chr2 | 44318602 | ||||||
chr2:44318603 | A | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2753T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2753 | chr2 | 44318603 | ||||||
chr2:44318604 | T | A | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2752A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2752 | chr2 | 44318604 | ||||||
chr2:44318604 | T | G | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2752A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2752 | chr2 | 44318604 | ||||||
chr2:44318605 | G | C | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2751C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2751 | chr2 | 44318605 | ||||||
chr2:44318606 | A | G | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2750T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2750 | chr2 | 44318606 | ||||||
chr2:44318607 | T | C | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2749A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2749 | chr2 | 44318607 | ||||||
chr2:44318609 | C | G | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2747G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2747 | chr2 | 44318609 | ||||||
chr2:44318610 | A | G | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2746T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2746 | chr2 | 44318610 | ||||||
chr2:44318611 | T | C | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2745A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2745 | chr2 | 44318611 | ||||||
chr2:44318611 | T | G | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2745A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2745 | chr2 | 44318611 | ||||||
chr2:44318612 | T | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2744A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2744 | chr2 | 44318612 | ||||||
chr2:44318613 | C | A | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2743G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2743 | chr2 | 44318613 | ||||||
chr2:44318614 | T | A | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2742A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2742 | chr2 | 44318614 | ||||||
chr2:44318615 | GTGCC | G | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2737_*2740delGGCA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2737 | chr2 | 44318615 | ||||||
chr2:44318616 | T | A | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2740A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2740 | chr2 | 44318616 | ||||||
chr2:44318617 | G | A | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2739C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2739 | chr2 | 44318617 | ||||||
chr2:44318618 | C | T | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2738G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2738 | chr2 | 44318618 | ||||||
chr2:44318619 | C | G | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2737G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2737 | chr2 | 44318619 | ||||||
chr2:44318623 | G | C | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2733C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2733 | chr2 | 44318623 | ||||||
chr2:44318624 | C | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2732G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2732 | chr2 | 44318624 | ||||||
chr2:44318625 | A | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2731T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2731 | chr2 | 44318625 | ||||||
chr2:44318626 | A | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2730T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2730 | chr2 | 44318626 | ||||||
chr2:44318627 | A | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2729T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2729 | chr2 | 44318627 | ||||||
chr2:44318637 | C | A | 3 | a0001c0001t0026 a0001c0001t0040 a0001c0001t0051 |
4 | HG02717.hp2 HG04115.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2719G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2719 | chr2 | 44318637 | ||||||
chr2:44318713 | T | C | 1 | a0001c0001t0052 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2643A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2643 | chr2 | 44318713 | ||||||
chr2:44318737 | T | C | 1 | a0002c0003t0033 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2619A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2619 | chr2 | 44318737 | ||||||
chr2:44318785 | G | C | 1 | a0001c0001t0039 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2571C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2571 | chr2 | 44318785 | ||||||
chr2:44318786 | C | G | 1 | a0001c0001t0039 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2570G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2570 | chr2 | 44318786 | ||||||
chr2:44318877 | C | T | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2479G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2479 | chr2 | 44318877 | ||||||
chr2:44319036 | CAT | C | 1 | a0001c0002t0017 | 3 | HG03130.hp2 HG03486.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2318_*2319delAT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2318 | chr2 | 44319036 | ||||||
chr2:44319145 | T | A | 1 | a0001c0001t0039 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2211 | chr2 | 44319145 | ||||||
chr2:44319232 | C | G | 1 | a0001c0001t0049 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2124G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2124 | chr2 | 44319232 | ||||||
chr2:44319264 | T | A | 1 | a0001c0002t0015 | 4 | HG02647.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2092A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2092 | chr2 | 44319264 | ||||||
chr2:44319287 | A | T | 1 | a0001c0001t0048 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2069T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 2069 | chr2 | 44319287 | ||||||
chr2:44319367 | T | C | 1 | a0001c0001t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1989A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1989 | chr2 | 44319367 | ||||||
chr2:44319454 | G | C | 1 | a0001c0010t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1902C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1902 | chr2 | 44319454 | ||||||
chr2:44319462 | C | A | 4 | a0002c0003t0020 a0002c0003t0033 a0004c0012t0032 others(1): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1894G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1894 | chr2 | 44319462 | ||||||
chr2:44319493 | CATTT | C | 2 | a0001c0001t0004 a0001c0001t0046 |
23 | HG00597.hp1 HG02056.hp1 HG02071.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1859_*1862delAAAT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1859 | chr2 | 44319493 | ||||||
chr2:44319562 | T | C | 1 | a0001c0001t0031 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1794 | chr2 | 44319562 | ||||||
chr2:44319602 | T | C | 26 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(23): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1754 | chr2 | 44319602 | ||||||
chr2:44319634 | T | A | 1 | a0001c0001t0038 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1722A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1722 | chr2 | 44319634 | ||||||
chr2:44319694 | T | C | 1 | a0001c0001t0011 | 7 | HG00544.hp1 HG02155.hp2 NA18943.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1662A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1662 | chr2 | 44319694 | ||||||
chr2:44319943 | A | T | 1 | a0001c0001t0047 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1413 | chr2 | 44319943 | ||||||
chr2:44319992 | A | G | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1364T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1364 | chr2 | 44319992 | ||||||
chr2:44320003 | A | G | 5 | a0001c0001t0009 a0001c0001t0036 a0001c0001t0038 others(2): Show |
11 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1353T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1353 | chr2 | 44320003 | ||||||
chr2:44320057 | A | T | 1 | a0001c0001t0046 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1299T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1299 | chr2 | 44320057 | ||||||
chr2:44320097 | G | C | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0022 others(1): Show |
19 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1259C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 1259 | chr2 | 44320097 | ||||||
chr2:44320427 | G | A | 1 | a0007c0014t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*929C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 929 | chr2 | 44320427 | ||||||
chr2:44320435 | G | A | 24 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(21): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*921C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 921 | chr2 | 44320435 | ||||||
chr2:44320770 | T | C | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(37): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*586A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 586 | chr2 | 44320770 | ||||||
chr2:44320865 | C | T | 1 | a0001c0001t0035 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 491 | chr2 | 44320865 | ||||||
chr2:44320886 | C | G | 1 | a0001c0001t0034 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 470 | chr2 | 44320886 | ||||||
chr2:44320958 | G | T | 4 | a0002c0003t0020 a0002c0003t0033 a0004c0012t0032 others(1): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*398C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 398 | chr2 | 44320958 | ||||||
chr2:44321143 | T | C | 54 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(51): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*213A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 213 | chr2 | 44321143 | ||||||
chr2:44321235 | C | T | 2 | a0001c0001t0016 a0001c0001t0055 |
4 | HG01168.hp2 HG01169.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*121G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 121 | chr2 | 44321235 | ||||||
chr2:44321342 | T | C | 1 | a0001c0001t0054 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 14/14 | 14 | chr2 | 44321342 | ||||||
chr2:44361397 | G | C | 2 | a0001c0001t0010 a0001c0001t0058 |
9 | HG00408.hp2 HG02523.hp2 NA18941.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-66C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | 15055 | chr2 | 44361397 | ||||||
chr2:44361426 | C | T | 1 | a0001c0001t0027 | 1 | HG01496.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | 15084 | chr2 | 44361426 | ||||||
chr2:44361455 | G | A | 1 | a0001c0001t0055 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | 15113 | chr2 | 44361455 | ||||||
chr2:44361486 | G | A | 3 | a0001c0001t0057 a0002c0003t0020 a0011c0013t0056 |
5 | HG02886.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | chr2 | 44361486 | |||||||
chr2:44361490 | T | G | 1 | a0001c0001t0058 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/14 | 15148 | chr2 | 44361490 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44321456 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1828-11G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 13/13 | chr2 | 44321456 | |||||||
chr2:44321474 | T | C | 165 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(162): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1828-29A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 13/13 | chr2 | 44321474 | |||||||
chr2:44321539 | C | T | 2 | a0001c0002t0017g0271 a0001c0002t0017g0272 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1828-94G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 13/13 | chr2 | 44321539 | |||||||
chr2:44321637 | C | T | 4 | a0001c0001t0040g0150 a0001c0010t0037g0151 a0003c0004t0009g0160 others(1): Show |
4 | HG00738.hp2 HG06807.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827+190G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 13/13 | chr2 | 44321637 | |||||||
chr2:44321922 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1754-22T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44321922 | |||||||
chr2:44322065 | A | G | 168 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(165): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1754-165T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322065 | |||||||
chr2:44322090 | G | A | 168 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(165): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1754-190C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322090 | |||||||
chr2:44322107 | G | A | 1 | a0001c0001t0039g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1754-207C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322107 | |||||||
chr2:44322168 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1754-268C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322168 | |||||||
chr2:44322185 | A | G | 4 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1754-285T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322185 | |||||||
chr2:44322392 | TTAGAGAT others(3): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1753+329_1753+338d others(12): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322392 | |||||||
chr2:44322403 | C | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1753+328G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322403 | |||||||
chr2:44322514 | C | A | 1 | a0001c0001t0019g0180 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1753+217G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322514 | |||||||
chr2:44322527 | G | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1753+204C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322527 | |||||||
chr2:44322596 | A | G | 3 | a0001c0001t0002g0036 a0001c0001t0002g0147 a0001c0001t0049g0214 |
4 | HG01069.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+135T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322596 | |||||||
chr2:44322645 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1753+86A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322645 | |||||||
chr2:44322730 | C | A | 1 | a0001c0001t0002g0039 | 2 | NA18945.hp1 NA19088.hp1 |
splice_donor_variant&intron_variant | HIGH | c.1753+1G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 12/13 | chr2 | 44322730 | |||||||
chr2:44322869 | A | G | 3 | a0001c0010t0037g0151 a0003c0004t0009g0160 a0003c0004t0009g0163 |
3 | HG00738.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1630-15T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44322869 | |||||||
chr2:44322880 | G | A | 1 | a0001c0001t0038g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1630-26C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44322880 | |||||||
chr2:44322948 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1630-94G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44322948 | |||||||
chr2:44322992 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1630-138C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44322992 | |||||||
chr2:44323094 | C | T | 147 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(144): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1629+168G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44323094 | |||||||
chr2:44323115 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1629+147G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44323115 | |||||||
chr2:44323128 | G | T | 4 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1629+134C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44323128 | |||||||
chr2:44323151 | A | G | 164 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(161): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1629+111T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 11/13 | chr2 | 44323151 | |||||||
chr2:44323463 | G | A | 1 | a0001c0001t0012g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1480-52C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323463 | |||||||
chr2:44323491 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0100 |
2 | NA18966.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1480-80A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323491 | |||||||
chr2:44323532 | A | C | 9 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(6): Show |
10 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1480-121T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323532 | |||||||
chr2:44323553 | C | A | 1 | a0001c0001t0029g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1480-142G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323553 | |||||||
chr2:44323643 | A | G | 1 | a0001c0001t0004g0185 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1480-232T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323643 | |||||||
chr2:44323779 | G | A | 3 | a0001c0001t0022g0171 a0001c0001t0022g0283 a0001c0001t0041g0281 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1480-368C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323779 | |||||||
chr2:44323798 | G | C | 20 | a0001c0001t0002g0183 a0001c0001t0002g0189 a0001c0001t0002g0211 others(17): Show |
28 | HG00597.hp1 HG01167.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.1480-387C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323798 | |||||||
chr2:44323846 | C | G | 1 | a0001c0001t0002g0205 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1480-435G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323846 | |||||||
chr2:44323909 | G | A | 1 | a0004c0012t0032g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1480-498C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44323909 | |||||||
chr2:44324465 | C | G | 3 | a0001c0001t0022g0171 a0001c0001t0022g0283 a0001c0001t0041g0281 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1480-1054G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44324465 | |||||||
chr2:44324804 | C | T | 4 | a0001c0001t0005g0040 a0001c0001t0005g0247 a0001c0001t0005g0250 others(1): Show |
5 | HG02698.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-1393G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44324804 | |||||||
chr2:44324842 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1480-1431C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44324842 | |||||||
chr2:44324953 | G | C | 1 | a0007c0014t0045g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1480-1542C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44324953 | |||||||
chr2:44325129 | G | T | 1 | a0001c0001t0054g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1479+1583C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325129 | |||||||
chr2:44325255 | T | C | 1 | a0002c0003t0033g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1479+1457A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325255 | |||||||
chr2:44325337 | G | A | 11 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(8): Show |
13 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1479+1375C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325337 | |||||||
chr2:44325419 | T | G | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1479+1293A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325419 | |||||||
chr2:44325428 | G | A | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1479+1284C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325428 | |||||||
chr2:44325558 | T | C | 1 | a0009c0009t0013g0192 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1479+1154A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325558 | |||||||
chr2:44325633 | G | T | 173 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(170): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1479+1079C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325633 | |||||||
chr2:44325693 | T | A | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 |
3 | HG00738.hp1 HG00741.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1479+1019A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325693 | |||||||
chr2:44325822 | T | C | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1479+890A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325822 | |||||||
chr2:44325861 | G | C | 1 | a0001c0002t0017g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1479+851C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325861 | |||||||
chr2:44325875 | C | T | 178 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(175): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1479+837G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325875 | |||||||
chr2:44325989 | T | C | 12 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(9): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1479+723A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44325989 | |||||||
chr2:44326138 | G | C | 5 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(2): Show |
6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1479+574C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326138 | |||||||
chr2:44326196 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1479+516T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326196 | |||||||
chr2:44326258 | C | G | 31 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(28): Show |
35 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1479+454G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326258 | |||||||
chr2:44326344 | T | C | 3 | a0001c0001t0002g0036 a0001c0001t0002g0147 a0001c0001t0049g0214 |
4 | HG01069.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+368A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326344 | |||||||
chr2:44326383 | C | CT | 14 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0002g0037 others(11): Show |
16 | HG01169.hp1 HG02135.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1479+328dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326383 | |||||||
chr2:44326383 | CT | C | 17 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0005g0253 others(14): Show |
19 | HG00099.hp2 HG00323.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1479+328delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326383 | |||||||
chr2:44326401 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0002g0219 |
2 | NA18959.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1479+311A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326401 | |||||||
chr2:44326428 | C | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0094 others(14): Show |
27 | HG00544.hp1 HG00673.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1479+284G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326428 | |||||||
chr2:44326457 | A | G | 3 | a0001c0001t0002g0194 a0001c0001t0044g0143 a0001c0001t0048g0195 |
3 | HG03017.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1479+255T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326457 | |||||||
chr2:44326495 | G | GT | 11 | a0001c0001t0005g0252 a0001c0001t0007g0016 a0001c0001t0007g0079 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1479+216dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326495 | |||||||
chr2:44326595 | G | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1479+117C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 10/13 | chr2 | 44326595 | |||||||
chr2:44326992 | G | C | 1 | a0001c0002t0017g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1263-64C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44326992 | |||||||
chr2:44327013 | G | GT | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1263-86dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327013 | |||||||
chr2:44327100 | G | C | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1263-172C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327100 | |||||||
chr2:44327163 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1263-235A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327163 | |||||||
chr2:44327198 | T | C | 1 | a0001c0001t0009g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1263-270A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327198 | |||||||
chr2:44327270 | T | G | 2 | a0001c0001t0040g0150 a0007c0014t0045g0243 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1263-342A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327270 | |||||||
chr2:44327585 | A | G | 182 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(179): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1263-657T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327585 | |||||||
chr2:44327617 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1263-689A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327617 | |||||||
chr2:44327638 | G | A | 1 | a0001c0001t0021g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1263-710C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327638 | |||||||
chr2:44327734 | G | A | 1 | a0001c0001t0024g0193 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1263-806C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327734 | |||||||
chr2:44327811 | G | A | 11 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1263-883C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327811 | |||||||
chr2:44327823 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1263-895T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327823 | |||||||
chr2:44327894 | A | C | 1 | a0001c0001t0002g0215 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1263-966T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327894 | |||||||
chr2:44327967 | T | A | 1 | a0001c0001t0003g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1262+970A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44327967 | |||||||
chr2:44328001 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1262+936T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328001 | |||||||
chr2:44328048 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1262+889C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328048 | |||||||
chr2:44328060 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1262+877G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328060 | |||||||
chr2:44328118 | G | T | 1 | a0001c0001t0013g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1262+819C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328118 | |||||||
chr2:44328237 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1262+700G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328237 | |||||||
chr2:44328260 | T | G | 8 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(5): Show |
9 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1262+677A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328260 | |||||||
chr2:44328268 | C | CA | 27 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(24): Show |
33 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1262+668dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328268 | |||||||
chr2:44328268 | C | CAAA | 133 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(130): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1262+666_1262+668d others(5): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328268 | |||||||
chr2:44328268 | C | CAAAA | 9 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0064 others(6): Show |
10 | HG00738.hp1 HG00741.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1262+665_1262+668d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328268 | |||||||
chr2:44328302 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1262+635A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328302 | |||||||
chr2:44328385 | C | T | 17 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(14): Show |
19 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1262+552G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328385 | |||||||
chr2:44328416 | G | A | 13 | a0001c0001t0003g0033 a0001c0001t0003g0167 a0001c0001t0003g0168 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1262+521C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328416 | |||||||
chr2:44328438 | C | CA | 26 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0059 others(23): Show |
29 | HG00438.hp1 HG00673.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.1262+498dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328438 | C | CAA | 108 | a0001c0001t0001g0060 a0001c0001t0001g0179 a0001c0001t0002g0001 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1262+497_1262+498d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328438 | C | CAAA | 34 | a0001c0001t0001g0139 a0001c0001t0002g0012 a0001c0001t0002g0038 others(31): Show |
38 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1262+496_1262+498d others(5): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328438 | CA | C | 8 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0003g0158 others(5): Show |
8 | HG01884.hp2 HG01975.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1262+498delT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328438 | CAA | C | 16 | a0001c0001t0003g0068 a0001c0001t0007g0015 a0001c0001t0007g0016 others(13): Show |
19 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1262+497_1262+498d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328438 | CAAAA | C | 8 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(5): Show |
9 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1262+495_1262+498d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328438 | |||||||
chr2:44328489 | G | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0197 a0001c0001t0002g0198 others(2): Show |
9 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+448C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328489 | |||||||
chr2:44328643 | A | G | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1262+294T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328643 | |||||||
chr2:44328835 | G | T | 1 | a0001c0001t0043g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1262+102C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328835 | |||||||
chr2:44328897 | G | T | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1262+40C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 9/13 | chr2 | 44328897 | |||||||
chr2:44329158 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1087-46T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329158 | |||||||
chr2:44329159 | T | C | 164 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(161): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1087-47A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329159 | |||||||
chr2:44329206 | C | A | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1087-94G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329206 | |||||||
chr2:44329240 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1087-128A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329240 | |||||||
chr2:44329373 | C | G | 18 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(15): Show |
20 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1087-261G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329373 | |||||||
chr2:44329582 | C | T | 4 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-470G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329582 | |||||||
chr2:44329649 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1087-537T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329649 | |||||||
chr2:44329803 | G | A | 19 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(16): Show |
22 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1087-691C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329803 | |||||||
chr2:44329914 | G | T | 11 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087-802C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329914 | |||||||
chr2:44329950 | C | T | 167 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(164): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1087-838G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329950 | |||||||
chr2:44329975 | A | C | 1 | a0001c0001t0043g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1087-863T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44329975 | |||||||
chr2:44330020 | C | A | 6 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(3): Show |
7 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087-908G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330020 | |||||||
chr2:44330246 | TAA | T | 20 | a0001c0001t0001g0139 a0001c0001t0002g0183 a0001c0001t0002g0189 others(17): Show |
28 | HG00597.hp1 HG01167.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.1087-1136_1087-113 others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330246 | |||||||
chr2:44330417 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1087-1305G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330417 | |||||||
chr2:44330542 | T | C | 12 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(9): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087-1430A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330542 | |||||||
chr2:44330607 | T | C | 1 | a0009c0009t0013g0192 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1087-1495A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330607 | |||||||
chr2:44330780 | C | T | 169 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(166): Show |
220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1087-1668G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330780 | |||||||
chr2:44330828 | G | A | 7 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086+1631C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330828 | |||||||
chr2:44330963 | G | A | 1 | a0001c0001t0010g0284 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1086+1496C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44330963 | |||||||
chr2:44331004 | G | A | 6 | a0001c0001t0002g0038 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
7 | HG00280.hp1 HG02280.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1086+1455C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331004 | |||||||
chr2:44331072 | A | G | 1 | a0001c0001t0054g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1086+1387T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331072 | |||||||
chr2:44331125 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1086+1334A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331125 | |||||||
chr2:44331132 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1086+1327C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331132 | |||||||
chr2:44331260 | G | C | 2 | a0001c0001t0002g0173 a0001c0001t0050g0229 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1086+1199C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331260 | |||||||
chr2:44331295 | A | G | 1 | a0001c0001t0029g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1086+1164T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331295 | |||||||
chr2:44331542 | A | G | 3 | a0001c0001t0022g0171 a0001c0001t0022g0283 a0001c0001t0041g0281 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1086+917T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331542 | |||||||
chr2:44331647 | C | T | 1 | a0008c0006t0002g0263 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1086+812G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331647 | |||||||
chr2:44331658 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0125 others(1): Show |
4 | NA18948.hp1 NA18961.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+801A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331658 | |||||||
chr2:44331946 | CT | C | 33 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0136 others(30): Show |
36 | HG00438.hp2 HG00597.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1086+512delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331946 | |||||||
chr2:44331946 | CTT | C | 135 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(132): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1086+511_1086+512d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331946 | |||||||
chr2:44331970 | G | A | 11 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1086+489C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44331970 | |||||||
chr2:44332032 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0077 others(7): Show |
15 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1086+427G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332032 | |||||||
chr2:44332033 | G | A | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1086+426C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332033 | |||||||
chr2:44332096 | G | A | 120 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(117): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1086+363C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332096 | |||||||
chr2:44332167 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1086+292G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332167 | |||||||
chr2:44332198 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1086+261C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332198 | |||||||
chr2:44332241 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1086+218G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332241 | |||||||
chr2:44332242 | G | A | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1086+217C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332242 | |||||||
chr2:44332339 | T | C | 5 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(2): Show |
6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+120A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332339 | |||||||
chr2:44332444 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1086+15C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 8/13 | chr2 | 44332444 | |||||||
chr2:44332757 | G | A | 7 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 others(4): Show |
7 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-101C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44332757 | |||||||
chr2:44332775 | C | T | 1 | a0001c0001t0006g0054 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.889-119G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44332775 | |||||||
chr2:44332816 | C | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.889-160G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44332816 | |||||||
chr2:44332981 | A | C | 6 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(3): Show |
7 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-325T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44332981 | |||||||
chr2:44333006 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.889-350G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333006 | |||||||
chr2:44333034 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.889-378A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333034 | |||||||
chr2:44333059 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.889-403C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333059 | |||||||
chr2:44333376 | A | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.889-720T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333376 | |||||||
chr2:44333425 | C | A | 1 | a0001c0001t0007g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.889-769G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333425 | |||||||
chr2:44333541 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.889-885G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333541 | |||||||
chr2:44333626 | T | TA | 161 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(158): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.889-971dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333626 | |||||||
chr2:44333700 | T | C | 1 | a0001c0001t0054g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.889-1044A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333700 | |||||||
chr2:44333714 | A | T | 3 | a0001c0001t0014g0022 a0001c0001t0014g0113 a0001c0001t0014g0120 |
4 | HG01074.hp2 HG01099.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1058T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333714 | |||||||
chr2:44333826 | A | G | 2 | a0001c0001t0040g0150 a0001c0010t0037g0151 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.889-1170T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333826 | |||||||
chr2:44333867 | T | A | 1 | a0006c0011t0006g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.889-1211A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333867 | |||||||
chr2:44333958 | T | C | 1 | a0001c0001t0014g0120 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.889-1302A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333958 | |||||||
chr2:44333961 | G | T | 4 | a0001c0001t0002g0170 a0001c0001t0002g0194 a0001c0001t0044g0143 others(1): Show |
4 | HG03017.hp1 HG03239.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1305C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333961 | |||||||
chr2:44333967 | C | T | 11 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(8): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.889-1311G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44333967 | |||||||
chr2:44334103 | G | A | 18 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(15): Show |
21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.889-1447C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334103 | |||||||
chr2:44334155 | T | G | 1 | a0001c0001t0004g0185 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.889-1499A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334155 | |||||||
chr2:44334183 | T | A | 1 | a0001c0001t0039g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.889-1527A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334183 | |||||||
chr2:44334195 | G | A | 3 | a0001c0001t0013g0076 a0002c0003t0033g0275 a0004c0012t0032g0276 |
3 | HG01884.hp2 HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.889-1539C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334195 | |||||||
chr2:44334199 | A | C | 21 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(18): Show |
23 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.889-1543T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334199 | |||||||
chr2:44334202 | T | C | 1 | a0002c0003t0020g0291 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.889-1546A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334202 | |||||||
chr2:44334242 | G | T | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.889-1586C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334242 | |||||||
chr2:44334393 | G | A | 139 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(136): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.889-1737C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334393 | |||||||
chr2:44334469 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.889-1813T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334469 | |||||||
chr2:44334475 | T | A | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.889-1819A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334475 | |||||||
chr2:44334488 | G | A | 156 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(153): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.889-1832C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334488 | |||||||
chr2:44334571 | A | T | 1 | a0007c0014t0045g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.889-1915T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334571 | |||||||
chr2:44334580 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.889-1924G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334580 | |||||||
chr2:44334588 | C | T | 1 | a0001c0002t0017g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.889-1932G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334588 | |||||||
chr2:44334614 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.889-1958G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334614 | |||||||
chr2:44334646 | A | G | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.889-1990T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334646 | |||||||
chr2:44334679 | C | G | 25 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(22): Show |
28 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-2023G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334679 | |||||||
chr2:44334734 | T | C | 1 | a0001c0001t0028g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.889-2078A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334734 | |||||||
chr2:44334744 | T | C | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889-2088A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334744 | |||||||
chr2:44334836 | T | C | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.889-2180A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334836 | |||||||
chr2:44334904 | C | A | 1 | a0001c0001t0007g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.889-2248G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334904 | |||||||
chr2:44334968 | C | T | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.889-2312G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334968 | |||||||
chr2:44334999 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.889-2343T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44334999 | |||||||
chr2:44335035 | T | C | 1 | a0001c0001t0055g0286 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889-2379A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335035 | |||||||
chr2:44335225 | C | A | 19 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(16): Show |
21 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.889-2569G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335225 | |||||||
chr2:44335374 | T | A | 1 | a0001c0001t0029g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.889-2718A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335374 | |||||||
chr2:44335395 | C | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(4): Show |
8 | HG00280.hp2 HG01070.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.889-2739G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335395 | |||||||
chr2:44335510 | A | G | 8 | a0001c0001t0013g0076 a0002c0003t0020g0289 a0002c0003t0020g0290 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+2841T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335510 | |||||||
chr2:44335590 | A | T | 19 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(16): Show |
21 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.888+2761T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335590 | |||||||
chr2:44335710 | A | C | 10 | a0001c0001t0013g0076 a0002c0003t0020g0289 a0002c0003t0020g0290 others(7): Show |
10 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.888+2641T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335710 | |||||||
chr2:44335712 | T | A | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+2639A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335712 | |||||||
chr2:44335748 | T | C | 1 | a0001c0001t0012g0279 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.888+2603A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335748 | |||||||
chr2:44335787 | T | A | 1 | a0001c0001t0002g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.888+2564A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335787 | |||||||
chr2:44335853 | A | C | 1 | a0001c0001t0004g0185 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.888+2498T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335853 | |||||||
chr2:44335930 | C | A | 1 | a0001c0001t0005g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.888+2421G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44335930 | |||||||
chr2:44336088 | G | C | 1 | a0001c0001t0005g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.888+2263C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336088 | |||||||
chr2:44336217 | T | C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.888+2134A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336217 | |||||||
chr2:44336224 | C | T | 8 | a0001c0001t0001g0179 a0001c0001t0002g0174 a0001c0001t0002g0175 others(5): Show |
8 | HG02056.hp2 NA18947.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.888+2127G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336224 | |||||||
chr2:44336263 | A | G | 1 | a0002c0003t0033g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.888+2088T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336263 | |||||||
chr2:44336423 | G | T | 1 | a0001c0001t0054g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.888+1928C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336423 | |||||||
chr2:44336699 | C | T | 2 | a0001c0001t0007g0015 a0001c0001t0007g0078 |
3 | HG01891.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.888+1652G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336699 | |||||||
chr2:44336790 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.888+1561A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336790 | |||||||
chr2:44336897 | T | C | 1 | a0007c0014t0045g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.888+1454A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44336897 | |||||||
chr2:44337112 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.888+1239A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337112 | |||||||
chr2:44337379 | A | G | 192 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0002g0001 others(189): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.888+972T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337379 | |||||||
chr2:44337460 | G | C | 7 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.888+891C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337460 | |||||||
chr2:44337665 | C | A | 19 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(16): Show |
21 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.888+686G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337665 | |||||||
chr2:44337748 | T | C | 6 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(3): Show |
7 | HG00280.hp2 HG01070.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.888+603A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337748 | |||||||
chr2:44337809 | G | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.888+542C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337809 | |||||||
chr2:44337811 | C | T | 4 | a0001c0001t0002g0170 a0001c0001t0002g0194 a0001c0001t0044g0143 others(1): Show |
4 | HG03017.hp1 HG03239.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+540G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337811 | |||||||
chr2:44337885 | G | A | 159 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(156): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.888+466C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337885 | |||||||
chr2:44337904 | C | G | 2 | a0001c0001t0040g0150 a0001c0010t0037g0151 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.888+447G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337904 | |||||||
chr2:44337985 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.888+366C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44337985 | |||||||
chr2:44338000 | G | A | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.888+351C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338000 | |||||||
chr2:44338055 | C | T | 160 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(157): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.888+296G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338055 | |||||||
chr2:44338127 | C | A | 157 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0012 others(154): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.888+224G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338127 | |||||||
chr2:44338154 | G | A | 137 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(134): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.888+197C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338154 | |||||||
chr2:44338184 | T | C | 22 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(19): Show |
24 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.888+167A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338184 | |||||||
chr2:44338205 | A | G | 1 | a0001c0001t0055g0286 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.888+146T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338205 | |||||||
chr2:44338213 | C | G | 2 | a0001c0001t0040g0150 a0001c0010t0037g0151 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.888+138G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338213 | |||||||
chr2:44338255 | G | C | 1 | a0001c0008t0001g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.888+96C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338255 | |||||||
chr2:44338308 | A | T | 159 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0012 others(156): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.888+43T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 7/13 | chr2 | 44338308 | |||||||
chr2:44338664 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.703-128C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44338664 | |||||||
chr2:44338872 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.702+275T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44338872 | |||||||
chr2:44338888 | G | A | 160 | a0001c0001t0001g0139 a0001c0001t0002g0001 a0001c0001t0002g0007 others(157): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.702+259C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44338888 | |||||||
chr2:44338957 | T | G | 5 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(2): Show |
6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+190A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44338957 | |||||||
chr2:44338988 | T | C | 1 | a0001c0001t0009g0084 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.702+159A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44338988 | |||||||
chr2:44339027 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.702+120A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44339027 | |||||||
chr2:44339049 | A | G | 1 | a0001c0001t0009g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.702+98T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 6/13 | chr2 | 44339049 | |||||||
chr2:44339440 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.486-77C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339440 | |||||||
chr2:44339493 | C | T | 1 | a0001c0001t0007g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-130G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339493 | |||||||
chr2:44339554 | G | C | 15 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(12): Show |
18 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.486-191C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339554 | |||||||
chr2:44339643 | T | C | 34 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0005g0040 others(31): Show |
36 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-280A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339643 | |||||||
chr2:44339645 | G | C | 1 | a0001c0001t0002g0037 | 2 | HG02486.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.486-282C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339645 | |||||||
chr2:44339678 | T | C | 1 | a0001c0001t0041g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.486-315A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339678 | |||||||
chr2:44339696 | C | A | 9 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0013g0076 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-333G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339696 | |||||||
chr2:44339733 | C | A | 5 | a0001c0001t0009g0017 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
6 | HG00280.hp2 HG01070.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-370G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339733 | |||||||
chr2:44339792 | C | G | 1 | a0004c0012t0032g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.486-429G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339792 | |||||||
chr2:44339867 | T | C | 33 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0005g0040 others(30): Show |
35 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.486-504A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339867 | |||||||
chr2:44339871 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486-508C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339871 | |||||||
chr2:44339890 | C | A | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-527G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339890 | |||||||
chr2:44339943 | C | T | 9 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0013g0076 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-580G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44339943 | |||||||
chr2:44340016 | ATG | A | 6 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(3): Show |
9 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-655_486-654del others(2): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340016 | |||||||
chr2:44340118 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.486-755T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340118 | |||||||
chr2:44340273 | CAATT | C | 4 | a0001c0001t0002g0170 a0001c0001t0002g0194 a0001c0001t0044g0143 others(1): Show |
4 | HG03017.hp1 HG03239.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-914_486-911del others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340273 | |||||||
chr2:44340344 | G | T | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-981C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340344 | |||||||
chr2:44340490 | C | T | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486-1127G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340490 | |||||||
chr2:44340738 | G | A | 2 | a0001c0001t0002g0173 a0001c0001t0050g0229 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.486-1375C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340738 | |||||||
chr2:44340758 | T | C | 1 | a0001c0001t0030g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.486-1395A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340758 | |||||||
chr2:44340799 | G | C | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-1436C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340799 | |||||||
chr2:44340833 | T | C | 49 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(46): Show |
54 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.486-1470A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340833 | |||||||
chr2:44340884 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.486-1521G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340884 | |||||||
chr2:44340885 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.486-1522C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340885 | |||||||
chr2:44340912 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.485+1505T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340912 | |||||||
chr2:44340921 | C | T | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+1496G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340921 | |||||||
chr2:44340927 | C | CAAAAAA | 7 | a0001c0001t0003g0167 a0001c0001t0005g0248 a0001c0001t0005g0250 others(4): Show |
7 | HG02735.hp1 HG02735.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+1484_485+1489d others(8): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340927 | |||||||
chr2:44340927 | C | CAAAAAAA | 24 | a0001c0001t0001g0264 a0001c0001t0003g0168 a0001c0001t0005g0040 others(21): Show |
26 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.485+1483_485+1489d others(9): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340927 | |||||||
chr2:44340927 | CA | C | 17 | a0001c0001t0001g0179 a0001c0001t0002g0177 a0001c0001t0002g0183 others(14): Show |
20 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+1489delT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44340927 | |||||||
chr2:44341015 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.485+1402A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341015 | |||||||
chr2:44341176 | C | T | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485+1241G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341176 | |||||||
chr2:44341242 | C | T | 15 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(12): Show |
18 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.485+1175G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341242 | |||||||
chr2:44341360 | A | G | 35 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(32): Show |
37 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.485+1057T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341360 | |||||||
chr2:44341399 | G | T | 1 | a0001c0001t0042g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.485+1018C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341399 | |||||||
chr2:44341462 | T | C | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485+955A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341462 | |||||||
chr2:44341555 | T | G | 35 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0005g0040 others(32): Show |
37 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.485+862A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341555 | |||||||
chr2:44341723 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.485+694G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341723 | |||||||
chr2:44341725 | A | G | 34 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(31): Show |
36 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+692T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341725 | |||||||
chr2:44341769 | T | C | 6 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0002c0003t0020g0289 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+648A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341769 | |||||||
chr2:44341777 | T | C | 2 | a0001c0001t0014g0022 a0001c0001t0014g0120 |
3 | HG01074.hp2 HG01099.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.485+640A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341777 | |||||||
chr2:44341779 | T | C | 34 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(31): Show |
36 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+638A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341779 | |||||||
chr2:44341824 | T | C | 17 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(14): Show |
20 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+593A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341824 | |||||||
chr2:44341830 | C | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0176 a0001c0001t0002g0200 |
4 | NA18969.hp2 NA18991.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+587G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341830 | |||||||
chr2:44341856 | C | G | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 |
3 | HG00738.hp1 HG00741.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.485+561G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341856 | |||||||
chr2:44341976 | G | C | 23 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(20): Show |
25 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+441C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341976 | |||||||
chr2:44341979 | C | G | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+438G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44341979 | |||||||
chr2:44342158 | A | G | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+259T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342158 | |||||||
chr2:44342189 | T | A | 140 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(137): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.485+228A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342189 | |||||||
chr2:44342334 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.485+83G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342334 | |||||||
chr2:44342335 | G | A | 181 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(178): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.485+82C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342335 | |||||||
chr2:44342379 | G | T | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+38C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342379 | |||||||
chr2:44342393 | G | T | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+24C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 5/13 | chr2 | 44342393 | |||||||
chr2:44342561 | AAAT | A | 143 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(140): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.350-12_350-10delAT others(1): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342561 | |||||||
chr2:44342600 | T | TA | 176 | a0001c0001t0001g0065 a0001c0001t0001g0148 a0001c0001t0002g0001 others(173): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.350-49dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342600 | |||||||
chr2:44342601 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.350-49T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342601 | |||||||
chr2:44342673 | A | G | 1 | a0001c0001t0011g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.350-121T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342673 | |||||||
chr2:44342706 | G | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.350-154C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342706 | |||||||
chr2:44342725 | T | C | 7 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-173A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342725 | |||||||
chr2:44342840 | A | G | 17 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(14): Show |
20 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.350-288T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342840 | |||||||
chr2:44342864 | T | C | 8 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0002c0003t0020g0289 others(5): Show |
8 | HG01884.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-312A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342864 | |||||||
chr2:44342942 | C | T | 19 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(16): Show |
21 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.350-390G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342942 | |||||||
chr2:44342963 | G | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0147 |
3 | HG01069.hp1 HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.350-411C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44342963 | |||||||
chr2:44343090 | A | G | 32 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(29): Show |
34 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.350-538T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343090 | |||||||
chr2:44343143 | G | A | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.350-591C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343143 | |||||||
chr2:44343373 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+372T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343373 | |||||||
chr2:44343443 | G | A | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.349+302C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343443 | |||||||
chr2:44343503 | G | C | 30 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(27): Show |
32 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.349+242C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343503 | |||||||
chr2:44343637 | C | T | 158 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(155): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.349+108G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343637 | |||||||
chr2:44343665 | C | A | 150 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(147): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.349+80G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 4/13 | chr2 | 44343665 | |||||||
chr2:44343970 | G | A | 20 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(17): Show |
22 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.143-19C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44343970 | |||||||
chr2:44344076 | CAAT | C | 150 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(147): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.143-128_143-126del others(3): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344076 | |||||||
chr2:44344136 | C | T | 10 | a0001c0002t0003g0155 a0001c0002t0003g0156 a0001c0002t0003g0157 others(7): Show |
12 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-185G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344136 | |||||||
chr2:44344268 | G | C | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+252C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344268 | |||||||
chr2:44344278 | T | C | 1 | a0001c0001t0006g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.142+242A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344278 | |||||||
chr2:44344321 | G | A | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02056.hp2 NA18955.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.142+199C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344321 | |||||||
chr2:44344436 | C | T | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142+84G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 3/13 | chr2 | 44344436 | |||||||
chr2:44344671 | A | T | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.76-85T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44344671 | |||||||
chr2:44344673 | ACT | A | 3 | a0001c0001t0007g0278 a0001c0001t0022g0283 a0001c0001t0041g0281 |
3 | HG02145.hp2 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.76-89_76-88delAG | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44344673 | |||||||
chr2:44344710 | G | A | 28 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0005g0040 others(25): Show |
30 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-124C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44344710 | |||||||
chr2:44345007 | T | A | 32 | a0001c0001t0001g0264 a0001c0001t0003g0167 a0001c0001t0003g0168 others(29): Show |
34 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.76-421A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345007 | |||||||
chr2:44345025 | C | T | 183 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0264 others(180): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.76-439G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345025 | |||||||
chr2:44345108 | T | A | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.76-522A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345108 | |||||||
chr2:44345281 | T | C | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.76-695A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345281 | |||||||
chr2:44345297 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.76-711A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345297 | |||||||
chr2:44345352 | A | AT | 21 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(18): Show |
23 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.76-767dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345352 | |||||||
chr2:44345352 | A | T | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.76-766T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345352 | |||||||
chr2:44345359 | C | T | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.76-773G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345359 | |||||||
chr2:44345364 | T | G | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.76-778A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345364 | |||||||
chr2:44345459 | C | A | 12 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0002t0003g0155 others(9): Show |
14 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+809G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345459 | |||||||
chr2:44345461 | C | G | 30 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(27): Show |
32 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.75+807G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345461 | |||||||
chr2:44345542 | T | A | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.75+726A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345542 | |||||||
chr2:44345590 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.75+678A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345590 | |||||||
chr2:44345645 | C | T | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.75+623G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345645 | |||||||
chr2:44345762 | T | A | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.75+506A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345762 | |||||||
chr2:44345908 | G | T | 22 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(19): Show |
24 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+360C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345908 | |||||||
chr2:44345920 | T | G | 1 | a0001c0001t0057g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+348A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345920 | |||||||
chr2:44345993 | T | A | 1 | a0001c0001t0007g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.75+275A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345993 | |||||||
chr2:44345998 | C | A | 2 | a0001c0001t0002g0224 a0001c0001t0034g0223 |
2 | NA18965.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.75+270G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345998 | |||||||
chr2:44345999 | G | A | 1 | a0001c0001t0029g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.75+269C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44345999 | |||||||
chr2:44346007 | T | C | 3 | a0001c0001t0002g0225 a0001c0001t0044g0143 a0001c0001t0048g0195 |
3 | HG02698.hp2 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+261A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44346007 | |||||||
chr2:44346021 | C | A | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.75+247G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44346021 | |||||||
chr2:44346028 | A | T | 1 | a0001c0001t0023g0249 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.75+240T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44346028 | |||||||
chr2:44346128 | TTTTAAG | T | 20 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(17): Show |
22 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.75+134_75+139delCT others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 2/13 | chr2 | 44346128 | |||||||
chr2:44346432 | G | C | 1 | a0001c0001t0007g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-48-42C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346432 | |||||||
chr2:44346485 | G | A | 165 | a0001c0001t0001g0148 a0001c0001t0001g0264 a0001c0001t0002g0001 others(162): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48-95C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346485 | |||||||
chr2:44346485 | G | C | 7 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48-95C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346485 | |||||||
chr2:44346486 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-48-96A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346486 | |||||||
chr2:44346519 | T | C | 186 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0264 others(183): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-48-129A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346519 | |||||||
chr2:44346532 | G | T | 166 | a0001c0001t0001g0148 a0001c0001t0001g0264 a0001c0001t0002g0001 others(163): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-48-142C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346532 | |||||||
chr2:44346574 | C | T | 1 | a0001c0001t0018g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-184G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346574 | |||||||
chr2:44346620 | T | C | 5 | a0001c0001t0001g0065 a0001c0001t0003g0074 a0001c0001t0006g0048 others(2): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-230A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346620 | |||||||
chr2:44346708 | A | G | 1 | a0001c0001t0005g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-48-318T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346708 | |||||||
chr2:44346724 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-48-334A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346724 | |||||||
chr2:44346924 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-48-534A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346924 | |||||||
chr2:44346957 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-48-567T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346957 | |||||||
chr2:44346967 | G | C | 2 | a0001c0001t0005g0255 a0001c0001t0005g0256 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-48-577C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44346967 | |||||||
chr2:44347056 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-48-666G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347056 | |||||||
chr2:44347057 | G | A | 1 | a0001c0001t0038g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48-667C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347057 | |||||||
chr2:44347123 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-48-733C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347123 | |||||||
chr2:44347138 | C | G | 107 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(104): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-48-748G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347138 | |||||||
chr2:44347152 | G | C | 27 | a0001c0001t0001g0065 a0001c0001t0003g0074 a0001c0001t0005g0261 others(24): Show |
31 | HG00280.hp2 HG01106.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-48-762C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347152 | |||||||
chr2:44347160 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-48-770C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347160 | |||||||
chr2:44347893 | C | T | 23 | a0001c0001t0001g0065 a0001c0001t0006g0048 a0001c0001t0006g0057 others(20): Show |
27 | HG00280.hp2 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-48-1503G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347893 | |||||||
chr2:44347932 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-48-1542A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347932 | |||||||
chr2:44347996 | T | C | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48-1606A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44347996 | |||||||
chr2:44348019 | G | C | 1 | a0001c0001t0005g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-48-1629C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348019 | |||||||
chr2:44348096 | C | T | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48-1706G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348096 | |||||||
chr2:44348157 | T | C | 1 | a0001c0001t0028g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-48-1767A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348157 | |||||||
chr2:44348229 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-48-1839A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348229 | |||||||
chr2:44348287 | C | T | 200 | a0001c0001t0001g0065 a0001c0001t0001g0148 a0001c0001t0002g0001 others(197): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-48-1897G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348287 | |||||||
chr2:44348809 | A | G | 3 | a0001c0001t0016g0030 a0001c0001t0022g0171 a0001c0001t0052g0181 |
4 | HG01168.hp1 HG01169.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-2419T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348809 | |||||||
chr2:44348910 | T | A | 1 | a0001c0001t0002g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-48-2520A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348910 | |||||||
chr2:44348936 | T | G | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-2546A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348936 | |||||||
chr2:44348939 | T | C | 6 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 others(3): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-2549A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348939 | |||||||
chr2:44348958 | A | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-48-2568T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44348958 | |||||||
chr2:44349278 | A | G | 185 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0264 others(182): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-48-2888T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349278 | |||||||
chr2:44349397 | G | A | 2 | a0001c0001t0003g0159 a0007c0014t0045g0243 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-48-3007C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349397 | |||||||
chr2:44349410 | C | T | 106 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(103): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-48-3020G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349410 | |||||||
chr2:44349477 | T | G | 1 | a0001c0001t0002g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-48-3087A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349477 | |||||||
chr2:44349636 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00544.hp2 HG02155.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-3246G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349636 | |||||||
chr2:44349691 | G | A | 7 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48-3301C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349691 | |||||||
chr2:44349703 | G | T | 4 | a0001c0001t0003g0033 a0001c0001t0013g0031 a0001c0001t0013g0191 others(1): Show |
6 | HG02717.hp1 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-3313C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349703 | |||||||
chr2:44349709 | A | G | 14 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(11): Show |
16 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48-3319T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349709 | |||||||
chr2:44349715 | G | A | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-48-3325C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349715 | |||||||
chr2:44349740 | G | C | 1 | a0001c0001t0030g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-48-3350C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349740 | |||||||
chr2:44349793 | G | A | 1 | a0001c0001t0002g0037 | 2 | HG02486.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-48-3403C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44349793 | |||||||
chr2:44350033 | T | A | 1 | a0001c0001t0038g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48-3643A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350033 | |||||||
chr2:44350278 | A | C | 1 | a0001c0001t0054g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-48-3888T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350278 | |||||||
chr2:44350286 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
55 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-48-3896C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350286 | |||||||
chr2:44350286 | G | C | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48-3896C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350286 | |||||||
chr2:44350321 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-3931T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350321 | |||||||
chr2:44350513 | AT | A | 13 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(10): Show |
16 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-4124delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350513 | |||||||
chr2:44350527 | G | A | 12 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0002t0003g0155 others(9): Show |
14 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-4137C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350527 | |||||||
chr2:44350665 | T | C | 2 | a0001c0001t0005g0261 a0001c0001t0005g0262 |
2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-48-4275A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350665 | |||||||
chr2:44350694 | C | T | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48-4304G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350694 | |||||||
chr2:44350733 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-48-4343C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350733 | |||||||
chr2:44350930 | C | T | 8 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-4540G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350930 | |||||||
chr2:44350965 | C | CT | 114 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(111): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-48-4576dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350965 | |||||||
chr2:44350982 | A | G | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48-4592T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350982 | |||||||
chr2:44350991 | C | T | 2 | a0001c0001t0007g0015 a0001c0001t0007g0078 |
3 | HG01891.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-48-4601G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44350991 | |||||||
chr2:44351030 | C | T | 1 | a0011c0013t0056g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48-4640G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351030 | |||||||
chr2:44351089 | A | AT | 7 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0270 others(4): Show |
7 | HG00597.hp2 HG01433.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-4700dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351089 | |||||||
chr2:44351089 | ATT | A | 48 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(45): Show |
52 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-48-4701_-48-4700d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351089 | |||||||
chr2:44351089 | ATTT | A | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-4702_-48-4700d others(5): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351089 | |||||||
chr2:44351141 | GC | G | 8 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-4752delG | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351141 | |||||||
chr2:44351167 | T | A | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-4777A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351167 | |||||||
chr2:44351214 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-48-4824G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351214 | |||||||
chr2:44351222 | A | T | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-4832T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351222 | |||||||
chr2:44351335 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-48-4945C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351335 | |||||||
chr2:44351339 | T | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-48-4949A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351339 | |||||||
chr2:44351340 | T | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-48-4950A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351340 | |||||||
chr2:44351356 | G | A | 1 | a0001c0001t0009g0084 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-48-4966C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351356 | |||||||
chr2:44351429 | A | ATT | 6 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 others(3): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-5040_-48-5039i others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351429 | |||||||
chr2:44351460 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-48-5070G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351460 | |||||||
chr2:44351470 | T | A | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48-5080A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351470 | |||||||
chr2:44351472 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0152 a0001c0001t0002g0153 |
4 | HG00438.hp2 HG00597.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-5082G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351472 | |||||||
chr2:44351487 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-48-5097T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351487 | |||||||
chr2:44351514 | T | TA | 10 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0006g0049 others(7): Show |
10 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48-5125dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351514 | |||||||
chr2:44351514 | TA | T | 138 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(135): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48-5125delT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351514 | |||||||
chr2:44351524 | A | C | 1 | a0001c0002t0017g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-48-5134T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351524 | |||||||
chr2:44351759 | T | C | 75 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(72): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-48-5369A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44351759 | |||||||
chr2:44352074 | T | C | 1 | a0001c0001t0011g0103 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-48-5684A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352074 | |||||||
chr2:44352077 | C | T | 1 | a0001c0001t0027g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-48-5687G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352077 | |||||||
chr2:44352091 | A | G | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48-5701T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352091 | |||||||
chr2:44352104 | A | G | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-5714T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352104 | |||||||
chr2:44352216 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-48-5826G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352216 | |||||||
chr2:44352332 | C | T | 17 | a0001c0001t0002g0183 a0001c0001t0002g0189 a0001c0001t0004g0006 others(14): Show |
25 | HG00597.hp1 HG01167.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.-48-5942G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352332 | |||||||
chr2:44352369 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0230 a0001c0001t0004g0233 |
7 | NA18948.hp2 NA18952.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-5979A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352369 | |||||||
chr2:44352404 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-48-6014A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352404 | |||||||
chr2:44352438 | T | G | 1 | a0001c0001t0010g0045 | 2 | NA18980.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-48-6048A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352438 | |||||||
chr2:44352502 | T | C | 1 | a0001c0001t0003g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48-6112A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352502 | |||||||
chr2:44352570 | T | C | 1 | a0001c0001t0005g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-48-6180A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352570 | |||||||
chr2:44352649 | G | C | 1 | a0001c0001t0006g0054 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48-6259C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352649 | |||||||
chr2:44352658 | C | G | 1 | a0001c0001t0005g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-48-6268G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352658 | |||||||
chr2:44352713 | A | G | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-6323T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352713 | |||||||
chr2:44352790 | A | G | 7 | a0001c0001t0001g0123 a0001c0001t0010g0044 a0001c0001t0010g0045 others(4): Show |
10 | HG00408.hp2 HG02523.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-6400T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352790 | |||||||
chr2:44352805 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-48-6415C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352805 | |||||||
chr2:44352858 | T | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
57 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-48-6468A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352858 | |||||||
chr2:44352930 | T | C | 200 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0179 others(197): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-48-6540A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352930 | |||||||
chr2:44352940 | A | G | 68 | a0001c0001t0001g0264 a0001c0001t0003g0008 a0001c0001t0003g0027 others(65): Show |
75 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-48-6550T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44352940 | |||||||
chr2:44353066 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG00673.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-48-6676C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353066 | |||||||
chr2:44353086 | A | T | 1 | a0001c0002t0003g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-48-6696T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353086 | |||||||
chr2:44353105 | G | A | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-6715C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353105 | |||||||
chr2:44353115 | G | C | 1 | a0001c0001t0012g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48-6725C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353115 | |||||||
chr2:44353262 | G | C | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-48-6872C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353262 | |||||||
chr2:44353384 | A | G | 1 | a0001c0001t0031g0061 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-48-6994T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353384 | |||||||
chr2:44353385 | G | A | 1 | a0001c0001t0031g0061 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-48-6995C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353385 | |||||||
chr2:44353413 | T | C | 155 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.-48-7023A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353413 | |||||||
chr2:44353495 | G | A | 105 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(102): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-48-7105C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353495 | |||||||
chr2:44353579 | C | T | 1 | a0001c0001t0013g0031 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-48-7189G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353579 | |||||||
chr2:44353587 | C | CA | 6 | a0001c0001t0002g0232 a0001c0001t0004g0233 a0001c0001t0054g0231 others(3): Show |
6 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-7198dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353587 | |||||||
chr2:44353594 | T | A | 161 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(158): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-48-7204A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353594 | |||||||
chr2:44353598 | T | A | 105 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(102): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-48-7208A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353598 | |||||||
chr2:44353649 | A | G | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-48-7259T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353649 | |||||||
chr2:44353718 | T | C | 1 | a0001c0001t0040g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48-7328A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353718 | |||||||
chr2:44353868 | A | G | 110 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(107): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-48-7478T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353868 | |||||||
chr2:44353876 | T | C | 37 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(34): Show |
40 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-48-7486A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353876 | |||||||
chr2:44353987 | C | A | 7 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+7393G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44353987 | |||||||
chr2:44354069 | C | T | 59 | a0001c0001t0003g0008 a0001c0001t0003g0027 a0001c0001t0003g0062 others(56): Show |
65 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.-49+7311G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354069 | |||||||
chr2:44354081 | A | G | 2 | a0003c0004t0009g0160 a0003c0004t0009g0163 |
2 | HG00738.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+7299T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354081 | |||||||
chr2:44354092 | G | A | 36 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(33): Show |
39 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.-49+7288C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354092 | |||||||
chr2:44354131 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+7249C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354131 | |||||||
chr2:44354170 | C | A | 15 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0002t0003g0155 others(12): Show |
17 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49+7210G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354170 | |||||||
chr2:44354181 | T | G | 1 | a0001c0001t0005g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+7199A>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354181 | |||||||
chr2:44354484 | A | G | 1 | a0001c0001t0057g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+6896T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354484 | |||||||
chr2:44354551 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-49+6829A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354551 | |||||||
chr2:44354578 | CT | C | 45 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(42): Show |
49 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49+6801delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354578 | |||||||
chr2:44354581 | T | C | 1 | a0001c0001t0007g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-49+6799A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354581 | |||||||
chr2:44354670 | G | A | 2 | a0001c0001t0026g0234 a0001c0001t0026g0235 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-49+6710C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354670 | |||||||
chr2:44354711 | A | G | 2 | a0001c0001t0019g0029 a0001c0001t0019g0180 |
3 | NA18999.hp1 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-49+6669T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354711 | |||||||
chr2:44354737 | G | A | 1 | a0001c0010t0037g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49+6643C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354737 | |||||||
chr2:44354857 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-49+6523C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354857 | |||||||
chr2:44354924 | G | A | 16 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(13): Show |
17 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49+6456C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44354924 | |||||||
chr2:44355134 | C | T | 242 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(239): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-49+6246G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355134 | |||||||
chr2:44355136 | G | C | 161 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(158): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-49+6244C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355136 | |||||||
chr2:44355145 | C | A | 1 | a0003c0004t0009g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-49+6235G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355145 | |||||||
chr2:44355152 | A | T | 1 | a0001c0001t0007g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-49+6228T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355152 | |||||||
chr2:44355213 | T | C | 1 | a0001c0001t0030g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-49+6167A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355213 | |||||||
chr2:44355311 | G | A | 1 | a0001c0001t0004g0149 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-49+6069C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355311 | |||||||
chr2:44355356 | A | G | 1 | a0001c0001t0003g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-49+6024T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355356 | |||||||
chr2:44355368 | G | A | 1 | a0001c0001t0038g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-49+6012C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355368 | |||||||
chr2:44355500 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-49+5880C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355500 | |||||||
chr2:44355524 | G | A | 16 | a0001c0001t0003g0074 a0001c0001t0003g0167 a0001c0001t0003g0168 others(13): Show |
18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.-49+5856C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355524 | |||||||
chr2:44355587 | C | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(1): Show |
6 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+5793G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355587 | |||||||
chr2:44355609 | C | T | 1 | a0002c0003t0033g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-49+5771G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355609 | |||||||
chr2:44355750 | A | ACTATATA others(5): Show |
1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-49+5629_-49+5630i others(14): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355750 | |||||||
chr2:44355751 | T | A | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-49+5629A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | T | TTA | 32 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0070 others(29): Show |
45 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-49+5627_-49+5628d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | T | TTATA | 12 | a0001c0001t0001g0025 a0001c0001t0001g0141 a0001c0001t0003g0167 others(9): Show |
14 | HG00438.hp1 HG02523.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-49+5625_-49+5628d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | T | TTATATA | 7 | a0001c0002t0003g0155 a0001c0002t0003g0156 a0001c0002t0003g0157 others(4): Show |
7 | HG00642.hp1 HG01099.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+5623_-49+5628d others(8): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | T | TTATATAT others(5): Show |
1 | a0001c0002t0003g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-49+5617_-49+5628d others(14): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | TTA | T | 31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0059 others(28): Show |
35 | HG00741.hp1 HG01192.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-49+5627_-49+5628d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | TTATA | T | 21 | a0001c0001t0001g0065 a0001c0001t0006g0048 a0001c0001t0006g0057 others(18): Show |
24 | HG00280.hp2 HG01106.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49+5625_-49+5628d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | TTATATA | T | 5 | a0001c0001t0002g0028 a0001c0001t0002g0176 a0001c0001t0002g0177 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+5623_-49+5628d others(8): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355751 | TTATATAT others(3): Show |
T | 7 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+5619_-49+5628d others(12): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355751 | |||||||
chr2:44355772 | TATATATA others(1): Show |
T | 10 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(7): Show |
12 | HG01243.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49+5600_-49+5607d others(10): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355772 | |||||||
chr2:44355774 | TATATAC | T | 105 | a0001c0001t0001g0148 a0001c0001t0002g0001 a0001c0001t0002g0007 others(102): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-49+5600_-49+5605d others(8): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355774 | |||||||
chr2:44355776 | TATAC | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0197 others(9): Show |
12 | HG00099.hp1 HG00621.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49+5600_-49+5603d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355776 | |||||||
chr2:44355778 | T | C | 14 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0078 others(11): Show |
17 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49+5602A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355778 | |||||||
chr2:44355780 | C | T | 17 | a0001c0001t0003g0074 a0001c0001t0003g0167 a0001c0001t0003g0168 others(14): Show |
19 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49+5600G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355780 | |||||||
chr2:44355792 | C | A | 1 | a0001c0001t0012g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-49+5588G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355792 | |||||||
chr2:44355925 | C | G | 4 | a0001c0001t0012g0043 a0001c0001t0012g0277 a0001c0001t0012g0279 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+5455G>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44355925 | |||||||
chr2:44356042 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-49+5338C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356042 | |||||||
chr2:44356069 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+5311C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356069 | |||||||
chr2:44356112 | T | C | 3 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 |
3 | HG02896.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49+5268A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356112 | |||||||
chr2:44356169 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18947.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-49+5211G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356169 | |||||||
chr2:44356200 | G | C | 199 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0264 others(196): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-49+5180C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356200 | |||||||
chr2:44356260 | G | C | 7 | a0001c0001t0006g0049 a0001c0001t0006g0050 a0001c0001t0006g0051 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+5120C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356260 | |||||||
chr2:44356285 | T | A | 6 | a0001c0001t0010g0044 a0001c0001t0010g0045 a0001c0001t0010g0046 others(3): Show |
9 | HG00408.hp2 HG02523.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+5095A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356285 | |||||||
chr2:44356325 | T | C | 1 | a0001c0001t0028g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49+5055A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356325 | |||||||
chr2:44356339 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-49+5041G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356339 | |||||||
chr2:44356415 | G | A | 7 | a0001c0001t0057g0287 a0002c0003t0020g0289 a0002c0003t0020g0290 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+4965C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356415 | |||||||
chr2:44356441 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-49+4939G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356441 | |||||||
chr2:44356514 | C | A | 15 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0002t0003g0155 others(12): Show |
17 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49+4866G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356514 | |||||||
chr2:44356515 | G | A | 2 | a0001c0001t0040g0150 a0001c0010t0037g0151 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-49+4865C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356515 | |||||||
chr2:44356534 | GACTCCGT others(13): Show |
G | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-49+4826_-49+4845d others(22): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356534 | |||||||
chr2:44356543 | T | TCAAA | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0008g0088 |
3 | HG02074.hp2 NA18939.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-49+4833_-49+4836d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356543 | |||||||
chr2:44356543 | TCAAA | T | 157 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(154): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-49+4833_-49+4836d others(6): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356543 | |||||||
chr2:44356543 | TCAAACAA others(5): Show |
T | 2 | a0001c0001t0054g0231 a0001c0010t0037g0151 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-49+4825_-49+4836d others(14): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356543 | |||||||
chr2:44356810 | A | AT | 36 | a0001c0001t0001g0077 a0001c0001t0001g0264 a0001c0001t0005g0040 others(33): Show |
41 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-49+4569dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356810 | |||||||
chr2:44356810 | AT | A | 157 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(154): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-49+4569delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356810 | |||||||
chr2:44356873 | AACCTCAC others(10): Show |
A | 6 | a0001c0001t0002g0038 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
7 | HG00280.hp1 HG02280.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+4490_-49+4506d others(19): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356873 | |||||||
chr2:44356874 | A | ACCTCACT others(4): Show |
56 | a0001c0001t0003g0008 a0001c0001t0003g0027 a0001c0001t0003g0062 others(53): Show |
62 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.-49+4495_-49+4505d others(13): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356874 | |||||||
chr2:44356879 | A | C | 1 | a0001c0001t0026g0235 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-49+4501T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356879 | |||||||
chr2:44356970 | A | C | 7 | a0001c0001t0057g0287 a0002c0003t0020g0289 a0002c0003t0020g0290 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+4410T>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44356970 | |||||||
chr2:44357017 | G | C | 4 | a0001c0001t0001g0065 a0001c0001t0006g0048 a0001c0001t0006g0057 others(1): Show |
4 | HG01106.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+4363C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357017 | |||||||
chr2:44357175 | G | A | 160 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0002g0001 others(157): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-49+4205C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357175 | |||||||
chr2:44357327 | G | T | 1 | a0002c0003t0033g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-49+4053C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357327 | |||||||
chr2:44357400 | C | T | 19 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0245 others(16): Show |
21 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49+3980G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357400 | |||||||
chr2:44357637 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-49+3743C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357637 | |||||||
chr2:44357829 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-49+3551A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357829 | |||||||
chr2:44357882 | G | T | 1 | a0001c0001t0013g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-49+3498C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357882 | |||||||
chr2:44357905 | G | T | 40 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(37): Show |
43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-49+3475C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44357905 | |||||||
chr2:44358067 | T | C | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+3313A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358067 | |||||||
chr2:44358188 | T | C | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+3192A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358188 | |||||||
chr2:44358383 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-49+2997G>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358383 | |||||||
chr2:44358383 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-49+2997G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358383 | |||||||
chr2:44358572 | A | G | 7 | a0001c0001t0057g0287 a0002c0003t0020g0289 a0002c0003t0020g0290 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+2808T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358572 | |||||||
chr2:44358584 | T | C | 7 | a0001c0001t0057g0287 a0002c0003t0020g0289 a0002c0003t0020g0290 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+2796A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358584 | |||||||
chr2:44358768 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-49+2612T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44358768 | |||||||
chr2:44359051 | T | C | 1 | a0007c0014t0045g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-49+2329A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359051 | |||||||
chr2:44359062 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0152 a0001c0001t0002g0153 |
4 | HG00438.hp2 HG00597.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+2318T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359062 | |||||||
chr2:44359067 | C | CT | 10 | a0001c0001t0001g0073 a0001c0001t0003g0074 a0001c0001t0005g0245 others(7): Show |
11 | HG00741.hp1 HG01109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-49+2312dupA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359067 | |||||||
chr2:44359067 | C | CTT | 7 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(4): Show |
9 | HG01243.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+2311_-49+2312d others(4): Show |
PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359067 | |||||||
chr2:44359067 | CT | C | 131 | a0001c0001t0001g0179 a0001c0001t0002g0001 a0001c0001t0002g0007 others(128): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-49+2312delA | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359067 | |||||||
chr2:44359088 | T | C | 1 | a0001c0002t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-49+2292A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359088 | |||||||
chr2:44359089 | C | T | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+2291G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359089 | |||||||
chr2:44359132 | G | A | 2 | a0002c0003t0033g0275 a0004c0012t0032g0276 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-49+2248C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359132 | |||||||
chr2:44359146 | G | A | 1 | a0001c0001t0002g0039 | 2 | NA18945.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-49+2234C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359146 | |||||||
chr2:44359475 | G | C | 1 | a0001c0001t0001g0269 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-49+1905C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359475 | |||||||
chr2:44359482 | T | C | 24 | a0001c0001t0001g0264 a0001c0001t0005g0040 a0001c0001t0005g0041 others(21): Show |
26 | HG00639.hp2 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49+1898A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359482 | |||||||
chr2:44359567 | T | A | 1 | a0001c0002t0003g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-49+1813A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359567 | |||||||
chr2:44359661 | G | A | 1 | a0002c0003t0020g0291 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-49+1719C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359661 | |||||||
chr2:44359762 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-49+1618G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359762 | |||||||
chr2:44359819 | G | A | 6 | a0002c0003t0020g0289 a0002c0003t0020g0290 a0002c0003t0020g0291 others(3): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+1561C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359819 | |||||||
chr2:44359988 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0060 others(1): Show |
6 | HG01934.hp2 HG01943.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+1392G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44359988 | |||||||
chr2:44360163 | A | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | NA18961.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-49+1217T>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360163 | |||||||
chr2:44360396 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-49+984C>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360396 | |||||||
chr2:44360397 | T | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+983A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360397 | |||||||
chr2:44360402 | T | TA | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+977dupT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360402 | |||||||
chr2:44360522 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+858G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360522 | |||||||
chr2:44360527 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-49+853A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360527 | |||||||
chr2:44360803 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49+577A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360803 | |||||||
chr2:44360806 | T | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+574A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360806 | |||||||
chr2:44360916 | T | C | 2 | a0001c0002t0017g0271 a0001c0002t0017g0272 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-49+464A>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360916 | |||||||
chr2:44360942 | GC | G | 5 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0003g0068 others(2): Show |
7 | HG01243.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49+437delG | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44360942 | |||||||
chr2:44361115 | T | A | 2 | a0001c0001t0018g0042 a0001c0001t0018g0273 |
3 | HG02647.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+265A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361115 | |||||||
chr2:44361146 | G | C | 1 | a0001c0001t0038g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-49+234C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361146 | |||||||
chr2:44361171 | T | A | 7 | a0001c0001t0057g0287 a0002c0003t0020g0289 a0002c0003t0020g0290 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+209A>T | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361171 | |||||||
chr2:44361278 | G | C | 8 | a0001c0001t0007g0278 a0001c0001t0012g0043 a0001c0001t0012g0277 others(5): Show |
9 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+102C>G | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361278 | |||||||
chr2:44361278 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+102C>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361278 | |||||||
chr2:44361367 | C | T | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 |
3 | HG00738.hp1 HG00741.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-49+13G>A | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361367 | |||||||
chr2:44361371 | CA | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0031g0061 |
4 | HG01934.hp2 HG01943.hp1 HG02148.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-49+8delT | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361371 | |||||||
chr2:44361376 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.-49+4T>C | PREPL | ENSG00000138078.16 | transcript | ENST00000409411.6 | protein_coding | 1/13 | chr2 | 44361376 |