Item | Value |
---|---|
geneid | 5817 |
ensemblid | ENSG00000073008.16 |
hgncid | 9705 |
symbol | PVR |
name | PVR cell adhesion molecule |
refseq_nuc | NM_006505.5 |
refseq_prot | NP_006496.4 |
ensembl_nuc | ENST00000425690.8 |
ensembl_prot | ENSP00000402060.2 |
mane_status | MANE Select |
chr | chr19 |
start | 44643910 |
end | 44666162 |
strand | + |
ver | v1.2 |
region | chr19:44643910-44666162 |
region5000 | chr19:44638910-44671162 |
regionname0 | PVR_chr19_44643910_44666162 |
regionname5000 | PVR_chr19_44638910_44671162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 417 | 313 | 61 | 61 | 139 | 13 | 37 | 103 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0002 | 0/0 | 417 | 63 | 4 | 12 | 39 | 1 | 7 | 35 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0003 | 0/0 | 417 | 23 | 22 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0004 | 0/0 | 417 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0005 | 0/0 | 417 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0006 | 0/0 | 417 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0007 | 0/0 | 417 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0008 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
a0009 | 0/0 | 416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | MARAM others(411): Show |
chr19 | 44638910 | 44671162 |
a0010 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | MARAM others(412): Show |
chr19 | 44638910 | 44671162 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1251 | 303 | 51 | 61 | 139 | 13 | 37 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0001c0004 | 0/0 | 1251 | 10 | 10 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0002c0002 | 0/0 | 1251 | 63 | 4 | 12 | 39 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0003c0003 | 0/0 | 1251 | 23 | 22 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0004c0006 | 0/0 | 1251 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0005c0005 | 0/0 | 1251 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0006c0007 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0006c0012 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0007c0010 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0008c0008 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 | ||
a0009c0009 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1243): Show |
chr19 | 44638910 | 44671162 | ||
a0010c0011 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | ATGGC others(1246): Show |
chr19 | 44638910 | 44671162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5791 | 49 | 2 | 3 | 37 | 2 | 5 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0002 | 0/0 | 5792 | 45 | 1 | 10 | 26 | 1 | 7 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0003 | 0/0 | 5792 | 27 | 0 | 6 | 16 | 2 | 3 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0004 | 0/0 | 5790 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0005 | 0/0 | 5793 | 18 | 2 | 6 | 7 | 0 | 3 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0006 | 0/0 | 5791 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0007 | 0/0 | 5792 | 10 | 6 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0008 | 0/0 | 5792 | 8 | 3 | 0 | 3 | 1 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0009 | 0/0 | 5793 | 8 | 0 | 1 | 4 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0010 | 0/0 | 5792 | 10 | 0 | 1 | 4 | 0 | 5 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0011 | 0/0 | 5792 | 7 | 0 | 0 | 7 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0012 | 1/0 | 5792 | 5 | 1 | 2 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0013 | 0/0 | 5792 | 5 | 1 | 3 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0014 | 0/0 | 5792 | 5 | 0 | 0 | 4 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0015 | 0/0 | 5792 | 5 | 0 | 4 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0017 | 0/0 | 5791 | 4 | 0 | 0 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0018 | 0/0 | 5793 | 4 | 0 | 3 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0019 | 0/0 | 5793 | 2 | 1 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0020 | 0/0 | 5794 | 3 | 0 | 3 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0021 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0022 | 0/0 | 5791 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0023 | 0/1 | 5794 | 3 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0024 | 0/0 | 5793 | 3 | 0 | 1 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0028 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0030 | 0/0 | 5791 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0031 | 0/0 | 5793 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0032 | 0/0 | 5782 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5777): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0033 | 0/0 | 5793 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0034 | 0/0 | 5794 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0036 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0037 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0038 | 0/0 | 5792 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0039 | 0/0 | 5787 | 2 | 1 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5782): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0040 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0041 | 0/0 | 5781 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5776): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0042 | 0/0 | 5780 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5775): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0043 | 0/0 | 5793 | 2 | 1 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0046 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5783): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0048 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0049 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0054 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0055 | 0/0 | 5793 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0057 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0058 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0059 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0060 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0063 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0064 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0065 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0066 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0067 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0068 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0069 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0070 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0072 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0073 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0074 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0075 | 0/0 | 5793 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0076 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0077 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0080 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0081 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0082 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0084 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0086 | 0/0 | 5792 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0087 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0088 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0089 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0090 | 0/0 | 5791 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0091 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5783): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0092 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0093 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0094 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0095 | 0/0 | 5789 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5784): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0096 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0097 | 0/0 | 5793 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0098 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0100 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0101 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0102 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0103 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0105 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0106 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0114 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0116 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0120 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5773): Show |
chr19 | 44638910 | 44671162 |
a0001c0001t0121 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0025 | 0/0 | 5790 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0026 | 0/0 | 5792 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0027 | 0/0 | 5791 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0050 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0051 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0052 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0001c0004t0053 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0003 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0004 | 0/0 | 5790 | 24 | 0 | 8 | 14 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0006 | 0/0 | 5791 | 14 | 0 | 2 | 11 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0008 | 0/0 | 5792 | 5 | 0 | 0 | 4 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0016 | 0/0 | 5792 | 5 | 1 | 0 | 2 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0019 | 0/0 | 5793 | 2 | 0 | 0 | 1 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0021 | 0/0 | 5791 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0022 | 0/0 | 5791 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0035 | 0/0 | 5791 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0036 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0061 | 0/0 | 5780 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5775): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0062 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0078 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0079 | 0/0 | 5762 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5757): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0083 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0002c0002t0085 | 0/0 | 5787 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5782): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0007 | 0/0 | 5792 | 4 | 3 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0044 | 0/0 | 5794 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0045 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0046 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5783): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0047 | 0/0 | 5793 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0104 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0107 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0108 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0109 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0110 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0111 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0112 | 0/0 | 5794 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0113 | 0/0 | 5792 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0115 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0117 | 0/0 | 5790 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0118 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0003c0003t0119 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0004c0006t0009 | 0/0 | 5793 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0004c0006t0034 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0005c0005t0002 | 0/0 | 5792 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
a0005c0005t0005 | 0/0 | 5793 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5788): Show |
chr19 | 44638910 | 44671162 |
a0006c0007t0029 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0006c0007t0056 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0006c0012t0029 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5786): Show |
chr19 | 44638910 | 44671162 |
a0007c0010t0071 | 0/0 | 5794 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5789): Show |
chr19 | 44638910 | 44671162 |
a0008c0008t0004 | 0/0 | 5790 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5785): Show |
chr19 | 44638910 | 44671162 |
a0009c0009t0099 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5829): Show |
chr19 | 44638910 | 44671162 |
a0010c0011t0002 | 0/0 | 5792 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | AGTCA others(5787): Show |
chr19 | 44638910 | 44671162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 19 | 1 | 1 | 14 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0003 | 0/0 | 15 | 0 | 2 | 13 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0001 | 0/0 | 16 | 0 | 2 | 9 | 2 | 3 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0004g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0001 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0002 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0012g0010 | 1/0 | 5 | 1 | 2 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0013g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0015g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0017g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0018g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0018g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0019g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0019g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0020g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0020g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0022g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0023g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0024g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0024g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0028g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0028g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0030g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0031g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0031g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0032g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0033g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0033g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0036g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0037g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0038g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0039g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0039g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0040g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0040g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0041g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0041g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0042g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0042g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0043g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0043g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0046g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0048g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0049g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0054g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0055g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0057g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0058g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0059g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0060g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0063g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0064g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0065g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0066g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0067g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0068g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0069g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0070g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0072g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0073g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0074g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0075g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0076g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0077g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0080g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0081g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0082g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0084g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0086g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0087g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0088g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0089g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0090g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0091g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0092g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0093g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0094g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0095g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0096g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0097g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0098g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0100g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0101g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0102g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0103g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0105g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0106g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0114g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0116g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0120g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0001t0121g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0025g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0026g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0027g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0050g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0051g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0052g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0001c0004t0053g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0004 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0016g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0019g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0021g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0022g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0035g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0036g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0061g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0062g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0078g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0079g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0083g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0002c0002t0085g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0044g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0045g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0045g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0046g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0047g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0104g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0107g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0108g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0109g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0110g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0111g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0112g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0113g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0115g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0117g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0118g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0003c0003t0119g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0004c0006t0009g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0004c0006t0034g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0005c0005t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0005c0005t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0006c0007t0029g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0006c0007t0056g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0006c0012t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0007c0010t0071g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0008c0008t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0009c0009t0099g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
a0010c0011t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00099 | hp2 | a0004 | c0006 | t0009 | g0001 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00140 | hp1 | a0002 | c0002 | t0022 | g0004 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00280 | hp1 | a0001 | c0001 | t0015 | g0013 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0166 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00323 | hp2 | a0001 | c0001 | t0018 | g0003 | EUR | FIN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00423 | hp1 | a0001 | c0001 | t0041 | g0062 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00423 | hp2 | a0001 | c0001 | t0017 | g0158 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00621 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00642 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00642 | hp2 | a0001 | c0001 | t0063 | g0012 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00733 | hp2 | a0001 | c0001 | t0070 | g0005 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00735 | hp1 | a0001 | c0001 | t0073 | g0152 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00735 | hp2 | a0004 | c0006 | t0034 | g0009 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00738 | hp1 | a0001 | c0001 | t0039 | g0118 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00741 | hp1 | a0001 | c0001 | t0023 | g0095 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01069 | hp2 | a0001 | c0001 | t0022 | g0156 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01070 | hp1 | a0001 | c0001 | t0015 | g0135 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0144 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01071 | hp1 | a0001 | c0001 | t0022 | g0001 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01071 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01074 | hp2 | a0001 | c0001 | t0033 | g0028 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01099 | hp1 | a0001 | c0001 | t0090 | g0019 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01109 | hp1 | a0001 | c0001 | t0088 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01109 | hp2 | a0003 | c0003 | t0007 | g0017 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01167 | hp2 | a0001 | c0001 | t0018 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01168 | hp1 | a0001 | c0001 | t0015 | g0136 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0013 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0164 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01175 | hp2 | a0001 | c0001 | t0010 | g0064 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01192 | hp2 | a0001 | c0001 | t0024 | g0094 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01243 | hp1 | a0001 | c0001 | t0020 | g0028 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01256 | hp2 | a0001 | c0001 | t0018 | g0005 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0013 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01257 | hp2 | a0002 | c0002 | t0006 | g0104 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01258 | hp1 | a0001 | c0001 | t0075 | g0013 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01258 | hp2 | a0001 | c0001 | t0018 | g0003 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01261 | hp1 | a0001 | c0001 | t0020 | g0013 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01261 | hp2 | a0001 | c0001 | t0020 | g0028 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01358 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01358 | hp2 | a0002 | c0002 | t0035 | g0004 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01361 | hp2 | a0002 | c0002 | t0035 | g0004 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0010 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01496 | hp1 | a0001 | c0001 | t0023 | g0096 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01516 | hp2 | a0001 | c0001 | t0024 | g0036 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01517 | hp1 | a0001 | c0001 | t0024 | g0036 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01517 | hp2 | a0004 | c0006 | t0009 | g0001 | EUR | IBS | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01884 | hp1 | a0001 | c0001 | t0120 | g0116 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01884 | hp2 | a0001 | c0001 | t0028 | g0087 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01891 | hp1 | a0001 | c0001 | t0038 | g0019 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01891 | hp2 | a0003 | c0003 | t0118 | g0092 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01928 | hp1 | a0002 | c0002 | t0006 | g0004 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01928 | hp2 | a0007 | c0010 | t0071 | g0012 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01943 | hp1 | a0001 | c0001 | t0031 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0022 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01993 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01993 | hp2 | a0001 | c0001 | t0030 | g0043 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02004 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02015 | hp1 | a0005 | c0005 | t0002 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02055 | hp1 | a0001 | c0001 | t0077 | g0137 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02055 | hp2 | a0002 | c0002 | t0036 | g0106 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02056 | hp1 | a0002 | c0002 | t0006 | g0004 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02071 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02074 | hp1 | a0001 | c0001 | t0100 | g0006 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0154 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02132 | hp2 | a0001 | c0001 | t0014 | g0170 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02135 | hp1 | a0001 | c0001 | t0010 | g0073 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02135 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02145 | hp1 | a0003 | c0003 | t0112 | g0011 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02155 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02155 | hp2 | a0001 | c0001 | t0066 | g0001 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02165 | hp1 | a0001 | c0001 | t0096 | g0002 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02165 | hp2 | a0001 | c0001 | t0065 | g0014 | EAS | CDX | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02257 | hp1 | a0003 | c0003 | t0047 | g0021 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02257 | hp2 | a0001 | c0001 | t0036 | g0025 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02258 | hp1 | a0003 | c0003 | t0115 | g0011 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02258 | hp2 | a0001 | c0001 | t0114 | g0086 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0103 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02280 | hp2 | a0001 | c0001 | t0028 | g0053 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02451 | hp1 | a0002 | c0002 | t0085 | g0060 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02451 | hp2 | a0001 | c0004 | t0027 | g0026 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02572 | hp1 | a0003 | c0003 | t0045 | g0011 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02572 | hp2 | a0001 | c0004 | t0026 | g0027 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02615 | hp1 | a0003 | c0003 | t0111 | g0034 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02622 | hp2 | a0001 | c0001 | t0106 | g0084 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02630 | hp1 | a0001 | c0001 | t0105 | g0085 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02630 | hp2 | a0001 | c0004 | t0052 | g0027 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02647 | hp1 | a0001 | c0004 | t0027 | g0128 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02647 | hp2 | a0001 | c0001 | t0043 | g0016 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02717 | hp1 | a0001 | c0001 | t0101 | g0006 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02717 | hp2 | a0001 | c0001 | t0094 | g0023 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02723 | hp1 | a0001 | c0004 | t0053 | g0026 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02723 | hp2 | a0001 | c0001 | t0082 | g0001 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0145 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02809 | hp1 | a0003 | c0003 | t0044 | g0017 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02809 | hp2 | a0002 | c0002 | t0083 | g0099 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02818 | hp1 | a0001 | c0001 | t0091 | g0117 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02818 | hp2 | a0003 | c0003 | t0007 | g0011 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02895 | hp1 | a0003 | c0003 | t0007 | g0088 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02896 | hp1 | a0001 | c0004 | t0025 | g0027 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02896 | hp2 | a0006 | c0007 | t0029 | g0125 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02897 | hp1 | a0001 | c0004 | t0025 | g0129 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02897 | hp2 | a0003 | c0003 | t0007 | g0089 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02922 | hp1 | a0003 | c0003 | t0117 | g0090 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02922 | hp2 | a0001 | c0001 | t0037 | g0025 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02965 | hp2 | a0006 | c0012 | t0029 | g0042 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02970 | hp1 | a0001 | c0004 | t0051 | g0127 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02970 | hp2 | a0003 | c0003 | t0119 | g0021 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03017 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03041 | hp1 | a0006 | c0007 | t0056 | g0042 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03041 | hp2 | a0001 | c0001 | t0072 | g0044 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03098 | hp1 | a0001 | c0004 | t0026 | g0153 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03098 | hp2 | a0003 | c0003 | t0108 | g0091 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03130 | hp2 | a0001 | c0001 | t0048 | g0126 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03139 | hp1 | a0003 | c0003 | t0107 | g0034 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03139 | hp2 | a0001 | c0001 | t0040 | g0023 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03195 | hp1 | a0001 | c0001 | t0058 | g0048 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03195 | hp2 | a0001 | c0001 | t0102 | g0006 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03209 | hp1 | a0003 | c0003 | t0045 | g0035 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03209 | hp2 | a0001 | c0001 | t0092 | g0023 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03225 | hp1 | a0001 | c0001 | t0069 | g0049 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03225 | hp2 | a0003 | c0003 | t0110 | g0098 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03453 | hp1 | a0001 | c0001 | t0040 | g0119 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03453 | hp2 | a0003 | c0003 | t0047 | g0021 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03486 | hp2 | a0003 | c0003 | t0044 | g0017 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03490 | hp1 | a0001 | c0001 | t0054 | g0168 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0123 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03491 | hp2 | a0001 | c0001 | t0086 | g0046 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03516 | hp1 | a0001 | c0001 | t0057 | g0048 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03516 | hp2 | a0001 | c0001 | t0074 | g0141 | AFR | ESN | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03540 | hp2 | a0001 | c0001 | t0039 | g0115 | AFR | GWD | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03654 | hp1 | a0002 | c0002 | t0016 | g0008 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0039 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03688 | hp2 | a0001 | c0001 | t0055 | g0030 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0039 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03710 | hp1 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03710 | hp2 | a0001 | c0001 | t0097 | g0002 | SAS | PJL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03831 | hp1 | a0002 | c0002 | t0016 | g0041 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03834 | hp1 | a0001 | c0001 | t0067 | g0003 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03834 | hp2 | a0001 | c0001 | t0030 | g0045 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03927 | hp2 | a0001 | c0001 | t0012 | g0010 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03942 | hp1 | a0001 | c0001 | t0034 | g0001 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03942 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04115 | hp1 | a0001 | c0001 | t0010 | g0032 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04115 | hp2 | a0001 | c0001 | t0095 | g0002 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0006 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04199 | hp2 | a0002 | c0002 | t0019 | g0101 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04228 | hp1 | a0002 | c0002 | t0008 | g0114 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG04228 | hp2 | a0001 | c0001 | t0033 | g0134 | SAS | STU | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18522 | hp1 | a0001 | c0001 | t0076 | g0049 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18522 | hp2 | a0003 | c0003 | t0109 | g0093 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18612 | hp1 | a0002 | c0002 | t0004 | g0113 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18747 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | CHB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18906 | hp1 | a0001 | c0004 | t0050 | g0026 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18906 | hp2 | a0001 | c0001 | t0059 | g0175 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18939 | hp1 | a0001 | c0001 | t0041 | g0020 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18939 | hp2 | a0001 | c0001 | t0032 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18941 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18942 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18945 | hp1 | a0001 | c0001 | t0116 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18945 | hp2 | a0002 | c0002 | t0016 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18946 | hp2 | a0002 | c0002 | t0021 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18947 | hp2 | a0002 | c0002 | t0006 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18949 | hp1 | a0002 | c0002 | t0016 | g0110 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18949 | hp2 | a0001 | c0001 | t0064 | g0014 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18950 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18951 | hp2 | a0002 | c0002 | t0006 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18953 | hp1 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18954 | hp1 | a0005 | c0005 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18956 | hp1 | a0001 | c0001 | t0049 | g0163 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18956 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18957 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18959 | hp1 | a0002 | c0002 | t0008 | g0102 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0143 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18965 | hp1 | a0002 | c0002 | t0004 | g0109 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0169 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18969 | hp2 | a0002 | c0002 | t0004 | g0107 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18970 | hp2 | a0002 | c0002 | t0008 | g0111 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18972 | hp1 | a0001 | c0001 | t0043 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18973 | hp2 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18975 | hp1 | a0002 | c0002 | t0078 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18975 | hp2 | a0002 | c0002 | t0006 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18977 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18979 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18979 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18980 | hp1 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18980 | hp2 | a0001 | c0001 | t0087 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18982 | hp1 | a0002 | c0002 | t0019 | g0105 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18983 | hp1 | a0001 | c0001 | t0042 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18989 | hp2 | a0002 | c0002 | t0079 | g0040 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18990 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18993 | hp2 | a0008 | c0008 | t0004 | g0038 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18994 | hp1 | a0001 | c0001 | t0010 | g0052 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18995 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA18999 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19000 | hp2 | a0001 | c0001 | t0081 | g0009 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19001 | hp1 | a0002 | c0002 | t0006 | g0108 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19002 | hp1 | a0002 | c0002 | t0062 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19003 | hp2 | a0001 | c0001 | t0098 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19006 | hp2 | a0001 | c0001 | t0060 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19010 | hp2 | a0002 | c0002 | t0021 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19030 | hp1 | a0003 | c0003 | t0104 | g0017 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19030 | hp2 | a0001 | c0001 | t0068 | g0177 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19043 | hp2 | a0001 | c0001 | t0089 | g0001 | AFR | LWK | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19054 | hp1 | a0002 | c0002 | t0006 | g0008 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19054 | hp2 | a0009 | c0009 | t0099 | g0079 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19058 | hp1 | a0001 | c0001 | t0042 | g0068 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19058 | hp2 | a0001 | c0001 | t0121 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19060 | hp1 | a0001 | c0001 | t0032 | g0046 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19064 | hp1 | a0002 | c0002 | t0004 | g0040 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19065 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19066 | hp1 | a0002 | c0002 | t0008 | g0120 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19067 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19068 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19068 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19072 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19072 | hp2 | a0001 | c0001 | t0080 | g0159 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19077 | hp1 | a0001 | c0001 | t0019 | g0024 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19077 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19078 | hp1 | a0002 | c0002 | t0006 | g0022 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19078 | hp2 | a0010 | c0011 | t0002 | g0178 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19079 | hp1 | a0002 | c0002 | t0006 | g0100 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19083 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19084 | hp1 | a0002 | c0002 | t0061 | g0121 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19084 | hp2 | a0002 | c0002 | t0006 | g0004 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19086 | hp2 | a0001 | c0001 | t0031 | g0031 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19088 | hp2 | a0002 | c0002 | t0008 | g0050 | EAS | JPT | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19240 | hp1 | a0001 | c0001 | t0038 | g0019 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | YRI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0139 | AFR | ASW | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20752 | hp2 | a0001 | c0001 | t0014 | g0018 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20805 | hp1 | a0001 | c0001 | t0009 | g0010 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20805 | hp2 | a0001 | c0001 | t0084 | g0001 | EUR | TSI | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20905 | hp1 | a0002 | c0002 | t0006 | g0041 | SAS | GIH | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | GIH | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01123 | hp1 | a0001 | c0001 | t0103 | g0171 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG01123 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | CLM | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02109 | hp1 | a0001 | c0001 | t0019 | g0174 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02109 | hp2 | a0001 | c0001 | t0093 | g0172 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02559 | hp1 | a0003 | c0003 | t0113 | g0011 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03471 | hp1 | a0002 | c0002 | t0016 | g0112 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG03471 | hp2 | a0001 | c0001 | t0037 | g0025 | AFR | MSL | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20300 | hp1 | a0001 | c0001 | t0046 | g0083 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
NA20300 | hp2 | a0003 | c0003 | t0046 | g0035 | AFR | USA | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0061 | REF | REF | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0010 | REF | REF | PVR_chr19_44638910_44671162 | PVR | chr19 | 44638910 | 44671162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44647342 | G | A | 2 | a0002 a0008 |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
missense_variant | MODERATE | c.199G>A | p.Ala67Thr | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/8 | 386/5792 | 199/1254 | 67/417 | chr19 | 44647342 | |||
chr19:44649958 | C | G | 1 | a0006 | 3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.577C>G | p.Pro193Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/8 | 764/5792 | 577/1254 | 193/417 | chr19 | 44649958 | |||
chr19:44650057 | G | A | 1 | a0005 | 3 | HG02015.hp1 HG02071.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.676G>A | p.Glu226Lys | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/8 | 863/5792 | 676/1254 | 226/417 | chr19 | 44650057 | |||
chr19:44653980 | C | G | 1 | a0008 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.805C>G | p.Arg269Gly | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/8 | 992/5792 | 805/1254 | 269/417 | chr19 | 44653980 | |||
chr19:44657802 | G | A | 1 | a0003 | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
missense_variant | MODERATE | c.883G>A | p.Ala295Thr | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1070/5792 | 883/1254 | 295/417 | chr19 | 44657802 | |||
chr19:44657831 | A | C | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.912A>C | p.Lys304Asn | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1099/5792 | 912/1254 | 304/417 | chr19 | 44657831 | |||
chr19:44657841 | A | G | 1 | a0007 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.922A>G | p.Thr308Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1109/5792 | 922/1254 | 308/417 | chr19 | 44657841 | |||
chr19:44658770 | G | A | 1 | a0004 | 3 | HG00099.hp2 HG00735.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.1020G>A | p.Met340Ile | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/8 | 1207/5792 | 1020/1254 | 340/417 | chr19 | 44658770 | |||
chr19:44661248 | CCAGCATT others(39): Show |
C | 1 | a0009 | 1 | NA19054.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1151-40_1156delCAT others(43): Show |
p.Ser384_Glu386delin others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/8 | 1151/1254 | 384/417 | INFO_REALIGN_3_PRIME | chr19 | 44661248 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44647491 | G | A | 1 | a0003c0003 | 23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
synonymous_variant | LOW | c.348G>A | p.Glu116Glu | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/8 | 535/5792 | 348/1254 | 116/417 | chr19 | 44647491 | |||
chr19:44653979 | T | A | 1 | a0006c0007 | 2 | HG02896.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.804T>A | p.Ala268Ala | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/8 | 991/5792 | 804/1254 | 268/417 | chr19 | 44653979 | |||
chr19:44657871 | C | T | 1 | a0001c0004 | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.952C>T | p.Leu318Leu | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/8 | 1139/5792 | 952/1254 | 318/417 | chr19 | 44657871 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44643944 | C | T | 1 | a0001c0001t0121 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | 153 | chr19 | 44643944 | ||||||
chr19:44643990 | AGGACCTG others(7): Show |
A | 1 | a0001c0001t0120 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103_-90delCCTGAGC others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | 90 | INFO_REALIGN_3_PRIME | chr19 | 44643990 | |||||
chr19:44644040 | G | T | 48 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(45): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/8 | chr19 | 44644040 | |||||||
chr19:44661968 | G | C | 1 | a0001c0001t0048 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 157 | chr19 | 44661968 | ||||||
chr19:44662053 | C | T | 1 | a0001c0001t0089 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 242 | chr19 | 44662053 | ||||||
chr19:44662231 | C | A | 1 | a0001c0001t0049 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 420 | chr19 | 44662231 | ||||||
chr19:44662246 | C | T | 1 | a0001c0001t0048 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 435 | chr19 | 44662246 | ||||||
chr19:44662259 | GT | G | 9 | a0001c0001t0038 a0001c0001t0090 a0001c0004t0025 others(6): Show |
13 | HG01099.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*454delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 454 | INFO_REALIGN_3_PRIME | chr19 | 44662259 | |||||
chr19:44662261 | T | G | 9 | a0001c0001t0038 a0001c0001t0090 a0001c0004t0025 others(6): Show |
13 | HG01099.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*450T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 450 | chr19 | 44662261 | ||||||
chr19:44662346 | C | G | 4 | a0003c0003t0047 a0003c0003t0117 a0003c0003t0118 others(1): Show |
5 | HG01891.hp2 HG02257.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 535 | chr19 | 44662346 | ||||||
chr19:44662645 | A | C | 137 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(134): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
3_prime_UTR_variant | MODIFIER | c.*834A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 834 | chr19 | 44662645 | ||||||
chr19:44662655 | A | G | 1 | a0001c0001t0088 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 844 | chr19 | 44662655 | ||||||
chr19:44662751 | T | C | 1 | a0001c0001t0054 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 940 | chr19 | 44662751 | ||||||
chr19:44662921 | G | A | 1 | a0001c0001t0028 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1110 | chr19 | 44662921 | ||||||
chr19:44663108 | G | C | 3 | a0001c0001t0039 a0001c0001t0091 a0001c0001t0120 |
4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1297G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1297 | chr19 | 44663108 | ||||||
chr19:44663135 | C | T | 1 | a0001c0004t0053 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1324 | chr19 | 44663135 | ||||||
chr19:44663180 | C | G | 1 | a0001c0001t0116 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1369 | chr19 | 44663180 | ||||||
chr19:44663185 | T | G | 2 | a0001c0001t0023 a0001c0001t0024 |
5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1374T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1374 | chr19 | 44663185 | ||||||
chr19:44663199 | G | A | 2 | a0001c0001t0013 a0001c0001t0055 |
6 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1388G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1388 | chr19 | 44663199 | ||||||
chr19:44663400 | A | G | 1 | a0003c0003t0115 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1589A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1589 | chr19 | 44663400 | ||||||
chr19:44663481 | G | A | 4 | a0001c0001t0048 a0006c0007t0029 a0006c0007t0056 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1670G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1670 | chr19 | 44663481 | ||||||
chr19:44663491 | G | A | 1 | a0001c0001t0089 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1680 | chr19 | 44663491 | ||||||
chr19:44663522 | G | A | 7 | a0001c0001t0040 a0001c0001t0057 a0001c0001t0058 others(4): Show |
8 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1711G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1711 | chr19 | 44663522 | ||||||
chr19:44663585 | C | T | 1 | a0001c0001t0087 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1774 | chr19 | 44663585 | ||||||
chr19:44663684 | C | T | 1 | a0001c0001t0086 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1873C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1873 | chr19 | 44663684 | ||||||
chr19:44663742 | CT | C | 15 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0041 others(12): Show |
74 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1942delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1942 | INFO_REALIGN_3_PRIME | chr19 | 44663742 | |||||
chr19:44663791 | G | A | 1 | a0002c0002t0062 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 1980 | chr19 | 44663791 | ||||||
chr19:44663847 | G | C | 1 | a0001c0001t0063 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2036 | chr19 | 44663847 | ||||||
chr19:44663948 | G | A | 3 | a0001c0001t0011 a0001c0001t0064 a0001c0001t0065 |
9 | HG00438.hp2 HG02165.hp2 NA18949.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2137G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2137 | chr19 | 44663948 | ||||||
chr19:44663975 | T | C | 1 | a0001c0001t0066 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2164 | chr19 | 44663975 | ||||||
chr19:44664149 | AAATT | A | 5 | a0001c0001t0039 a0001c0001t0046 a0001c0001t0091 others(2): Show |
6 | HG00738.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344_*2347delATTA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2344 | INFO_REALIGN_3_PRIME | chr19 | 44664149 | |||||
chr19:44664264 | A | G | 50 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(47): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2453A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2453 | chr19 | 44664264 | ||||||
chr19:44664357 | C | T | 1 | a0001c0001t0084 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2546 | chr19 | 44664357 | ||||||
chr19:44664435 | A | G | 1 | a0001c0001t0114 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2624A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2624 | chr19 | 44664435 | ||||||
chr19:44664491 | A | C | 23 | a0001c0001t0046 a0001c0001t0048 a0001c0001t0076 others(20): Show |
23 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2680A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2680 | chr19 | 44664491 | ||||||
chr19:44664502 | C | G | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0033 others(1): Show |
11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2691C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2691 | chr19 | 44664502 | ||||||
chr19:44664711 | C | CT | 11 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0074 others(8): Show |
14 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2914dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2915 | INFO_REALIGN_3_PRIME | chr19 | 44664711 | |||||
chr19:44664711 | CT | C | 20 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0015 others(17): Show |
68 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2914delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 2914 | INFO_REALIGN_3_PRIME | chr19 | 44664711 | |||||
chr19:44664826 | A | T | 3 | a0001c0001t0046 a0002c0002t0085 a0003c0003t0046 |
3 | HG02451.hp1 NA20300.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3015A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3015 | chr19 | 44664826 | ||||||
chr19:44664895 | A | G | 1 | a0001c0001t0059 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3084 | chr19 | 44664895 | ||||||
chr19:44664963 | T | C | 4 | a0001c0001t0068 a0001c0001t0069 a0001c0001t0076 others(1): Show |
4 | HG01123.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3152T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3152 | chr19 | 44664963 | ||||||
chr19:44665105 | A | G | 1 | a0001c0001t0081 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3294A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3294 | chr19 | 44665105 | ||||||
chr19:44665131 | G | A | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0033 others(1): Show |
11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3320G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3320 | chr19 | 44665131 | ||||||
chr19:44665156 | C | CG | 5 | a0001c0001t0018 a0001c0001t0023 a0001c0001t0024 others(2): Show |
11 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3351dupG | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3352 | INFO_REALIGN_3_PRIME | chr19 | 44665156 | |||||
chr19:44665156 | C | T | 3 | a0003c0003t0045 a0003c0003t0108 a0003c0003t0113 |
4 | HG02559.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3345C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3345 | chr19 | 44665156 | ||||||
chr19:44665157 | G | A | 1 | a0001c0001t0070 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3346G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3346 | chr19 | 44665157 | ||||||
chr19:44665196 | C | T | 1 | a0001c0001t0072 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3385C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3385 | chr19 | 44665196 | ||||||
chr19:44665230 | G | A | 16 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0014 others(13): Show |
56 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3419G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3419 | chr19 | 44665230 | ||||||
chr19:44665466 | C | G | 4 | a0001c0001t0105 a0001c0001t0106 a0003c0003t0112 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3655C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3655 | chr19 | 44665466 | ||||||
chr19:44665467 | G | A | 1 | a0002c0002t0078 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3656G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3656 | chr19 | 44665467 | ||||||
chr19:44665574 | G | C | 14 | a0001c0001t0028 a0001c0001t0046 a0001c0004t0025 others(11): Show |
18 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3763G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3763 | chr19 | 44665574 | ||||||
chr19:44665619 | AGT | A | 3 | a0001c0001t0068 a0001c0001t0076 a0001c0001t0103 |
3 | HG01123.hp1 NA18522.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3810_*3811delTG | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3810 | INFO_REALIGN_3_PRIME | chr19 | 44665619 | |||||
chr19:44665635 | C | CA | 30 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0010 others(27): Show |
82 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3849dupA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3850 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | |||||
chr19:44665635 | C | CAA | 13 | a0001c0001t0020 a0001c0001t0034 a0001c0001t0057 others(10): Show |
15 | HG00735.hp2 HG01123.hp1 HG01243.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3848_*3849dupAA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3850 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | |||||
chr19:44665635 | CA | C | 31 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0022 others(28): Show |
63 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3849delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3849 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | |||||
chr19:44665635 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0032 a0001c0001t0041 |
4 | HG00423.hp1 NA18939.hp1 NA18939.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3840_*3849delAAAA others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3840 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | |||||
chr19:44665635 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0042 a0002c0002t0061 |
3 | NA18983.hp1 NA19058.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3839_*3849delAAAA others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3839 | INFO_REALIGN_3_PRIME | chr19 | 44665635 | |||||
chr19:44665670 | C | T | 1 | a0001c0001t0100 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3859C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3859 | chr19 | 44665670 | ||||||
chr19:44665681 | C | CTTTTTTA others(39): Show |
1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3870_*3871insTTTT others(42): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3871 | chr19 | 44665681 | ||||||
chr19:44665683 | G | T | 1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3872G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3872 | chr19 | 44665683 | ||||||
chr19:44665686 | C | T | 1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3875C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3875 | chr19 | 44665686 | ||||||
chr19:44665687 | A | T | 1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3876 | chr19 | 44665687 | ||||||
chr19:44665688 | C | G | 1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3877C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3877 | chr19 | 44665688 | ||||||
chr19:44665694 | G | T | 1 | a0009c0009t0099 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3883G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3883 | chr19 | 44665694 | ||||||
chr19:44665701 | C | T | 1 | a0001c0001t0092 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3890C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3890 | chr19 | 44665701 | ||||||
chr19:44665757 | TGGTGCCA others(22): Show |
T | 1 | a0002c0002t0079 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3947_*3975delGGTG others(25): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 3947 | chr19 | 44665757 | ||||||
chr19:44665943 | C | A | 1 | a0001c0001t0098 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4132C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4132 | chr19 | 44665943 | ||||||
chr19:44665957 | C | T | 2 | a0003c0003t0107 a0003c0003t0111 |
2 | HG02615.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4146C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4146 | chr19 | 44665957 | ||||||
chr19:44665974 | C | A | 1 | a0003c0003t0113 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4163C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4163 | chr19 | 44665974 | ||||||
chr19:44666140 | A | T | 1 | a0002c0002t0035 | 2 | HG01358.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4329A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 8/8 | 4329 | chr19 | 44666140 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:44644235 | C | G | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.79+60C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644235 | |||||||
chr19:44644272 | C | T | 7 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(4): Show |
7 | HG03130.hp1 HG03195.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+97C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644272 | |||||||
chr19:44644307 | G | T | 2 | a0001c0001t0008g0173 a0001c0001t0019g0174 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+132G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644307 | |||||||
chr19:44644386 | A | T | 2 | a0001c0001t0093g0172 a0001c0001t0103g0171 |
2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.79+211A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644386 | |||||||
chr19:44644419 | T | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(134): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.79+244T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644419 | |||||||
chr19:44644420 | C | G | 2 | a0002c0002t0008g0120 a0002c0002t0061g0121 |
2 | NA19066.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.79+245C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644420 | |||||||
chr19:44644468 | G | A | 3 | a0002c0002t0008g0050 a0002c0002t0008g0120 a0002c0002t0061g0121 |
3 | NA19066.hp1 NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79+293G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644468 | |||||||
chr19:44644612 | G | T | 6 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(3): Show |
6 | HG01123.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+437G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644612 | |||||||
chr19:44644676 | A | G | 6 | a0001c0001t0014g0169 a0001c0001t0014g0170 a0001c0001t0039g0115 others(3): Show |
6 | HG00738.hp1 HG01884.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+501A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644676 | |||||||
chr19:44644692 | G | T | 1 | a0001c0001t0054g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79+517G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644692 | |||||||
chr19:44644719 | CT | C | 6 | a0001c0001t0001g0051 a0001c0001t0002g0122 a0001c0001t0003g0124 others(3): Show |
6 | HG01074.hp1 HG02280.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+560delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44644719 | ||||||
chr19:44644818 | C | A | 1 | a0001c0001t0007g0054 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.79+643C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644818 | |||||||
chr19:44644819 | G | A | 2 | a0001c0001t0008g0024 a0001c0001t0019g0024 |
3 | HG00609.hp1 NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.79+644G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644819 | |||||||
chr19:44644850 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.79+675G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644850 | |||||||
chr19:44644925 | C | A | 2 | a0001c0001t0036g0025 a0001c0001t0037g0025 |
3 | HG02257.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79+750C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44644925 | |||||||
chr19:44645003 | TA | T | 40 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(37): Show |
63 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.79+833delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645003 | ||||||
chr19:44645004 | AAAAATAT others(34): Show |
A | 1 | a0001c0001t0065g0014 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.79+909_79+949delAA others(39): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645004 | ||||||
chr19:44645057 | T | C | 5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+882T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645057 | |||||||
chr19:44645068 | GTAATATA | G | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+906_79+912delTA others(5): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645068 | ||||||
chr19:44645080 | A | G | 1 | a0003c0003t0110g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+905A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645080 | |||||||
chr19:44645083 | TAA | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+909_79+910delAA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645083 | |||||||
chr19:44645088 | A | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+913A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645088 | |||||||
chr19:44645098 | T | C | 5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+923T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645098 | |||||||
chr19:44645100 | T | TATTATAA others(6): Show |
1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+927_79+928insTA others(11): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645100 | ||||||
chr19:44645106 | ATAG | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+934_79+936delGT others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645106 | ||||||
chr19:44645107 | TA | T | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+933delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645107 | |||||||
chr19:44645108 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+933A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645108 | |||||||
chr19:44645109 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+934G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645109 | |||||||
chr19:44645119 | A | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.79+944A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645119 | |||||||
chr19:44645121 | ATATTATA others(55): Show |
A | 2 | a0002c0002t0003g0038 a0008c0008t0004g0038 |
2 | NA18950.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.79+960_79+1021delT others(61): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645121 | ||||||
chr19:44645122 | TA | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+948delA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645122 | |||||||
chr19:44645123 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+948A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645123 | |||||||
chr19:44645124 | T | G | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+949T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645124 | |||||||
chr19:44645124 | T | TAATAAAA others(71): Show |
5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+949_79+950insAA others(76): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645124 | |||||||
chr19:44645128 | A | AATATATA others(33): Show |
8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(38): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | AATATATA others(30): Show |
47 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0037 others(44): Show |
58 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(35): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | AATATATA others(70): Show |
15 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0033 others(12): Show |
24 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(75): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | AATATATA others(68): Show |
4 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0091g0117 others(1): Show |
4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+959_79+960insAA others(73): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | AATATATT others(30): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0071 others(4): Show |
14 | HG00597.hp2 HG00673.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+971_79+972insAA others(35): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | AATATATT others(33): Show |
2 | a0001c0004t0026g0153 a0001c0004t0027g0128 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+1031_79+1070dup others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645128 | A | T | 6 | a0001c0001t0001g0097 a0001c0001t0007g0016 a0001c0001t0007g0057 others(3): Show |
8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+953A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645128 | |||||||
chr19:44645128 | AATATATT others(33): Show |
A | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0045 others(41): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.79+1031_79+1070del others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645128 | ||||||
chr19:44645129 | A | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+954A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645129 | |||||||
chr19:44645135 | T | A | 73 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(70): Show |
102 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(99): Show |
intron_variant | MODIFIER | c.79+960T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645135 | |||||||
chr19:44645136 | A | ATATATAT others(28): Show |
4 | a0001c0001t0023g0095 a0001c0001t0023g0096 a0001c0001t0024g0036 others(1): Show |
5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+971_79+972insAA others(33): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645136 | ||||||
chr19:44645136 | A | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+961A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645136 | |||||||
chr19:44645137 | T | TA | 54 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(51): Show |
80 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.79+963dupA | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645137 | ||||||
chr19:44645140 | ATAT | A | 10 | a0003c0003t0007g0017 a0003c0003t0007g0088 a0003c0003t0007g0089 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+972_79+974delTA others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645140 | ||||||
chr19:44645142 | AT | A | 54 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(51): Show |
80 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.79+969delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645142 | ||||||
chr19:44645162 | G | A | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+987G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645162 | |||||||
chr19:44645163 | T | C | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+988T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645163 | |||||||
chr19:44645178 | AT | A | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1004delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645178 | |||||||
chr19:44645183 | T | A | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1008T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645183 | |||||||
chr19:44645183 | T | TTATTATT others(30): Show |
38 | a0002c0002t0004g0004 a0002c0002t0004g0007 a0002c0002t0004g0022 others(35): Show |
59 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.79+1014_79+1015ins others(37): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645183 | ||||||
chr19:44645183 | T | TTATTATT others(67): Show |
1 | a0002c0002t0004g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.79+1014_79+1015ins others(74): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645183 | ||||||
chr19:44645186 | T | TA | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1011_79+1012ins others(1): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645186 | |||||||
chr19:44645187 | T | A | 1 | a0001c0001t0041g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+1012T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645187 | |||||||
chr19:44645192 | T | A | 1 | a0001c0001t0041g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+1017T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645192 | |||||||
chr19:44645202 | G | A | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1027G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645202 | |||||||
chr19:44645203 | T | C | 4 | a0001c0001t0048g0126 a0006c0007t0029g0125 a0006c0007t0056g0042 others(1): Show |
4 | HG02896.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1028T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645203 | |||||||
chr19:44645227 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(127): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.79+1052T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645227 | |||||||
chr19:44645227 | T | TATAATAT others(33): Show |
5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1070_79+1071ins others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645227 | ||||||
chr19:44645232 | T | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(46): Show |
78 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.79+1057T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645232 | |||||||
chr19:44645232 | T | TATATAAT others(33): Show |
1 | a0001c0001t0001g0037 | 2 | NA18965.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.79+1070_79+1071ins others(40): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645232 | ||||||
chr19:44645276 | ATAT | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1102_79+1104del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645276 | |||||||
chr19:44645285 | TTAA | T | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+1114_79+1116del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645285 | ||||||
chr19:44645303 | ATATAT | A | 6 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1134_79+1138del others(5): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645303 | ||||||
chr19:44645404 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.79+1229A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645404 | |||||||
chr19:44645413 | G | GTATATAT others(5): Show |
1 | a0001c0001t0046g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+1239_79+1240ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | ||||||
chr19:44645413 | G | GTATATAT others(7): Show |
4 | a0001c0004t0027g0026 a0001c0004t0050g0026 a0001c0004t0051g0127 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1239_79+1240ins others(14): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | ||||||
chr19:44645413 | G | GTATATAT others(9): Show |
5 | a0001c0004t0025g0027 a0001c0004t0025g0129 a0001c0004t0026g0027 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1239_79+1240ins others(16): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | ||||||
chr19:44645413 | GTGTATAT others(1): Show |
G | 3 | a0002c0002t0006g0008 a0002c0002t0016g0008 a0002c0002t0021g0008 |
6 | HG03654.hp1 NA18946.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1240_79+1247del others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | ||||||
chr19:44645413 | GTGTATAT others(3): Show |
G | 37 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(34): Show |
57 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.79+1240_79+1249del others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645413 | ||||||
chr19:44645415 | G | A | 12 | a0001c0001t0046g0083 a0001c0001t0114g0086 a0001c0004t0025g0027 others(9): Show |
12 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+1240G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645415 | |||||||
chr19:44645415 | G | GTA | 11 | a0001c0001t0002g0012 a0001c0001t0002g0148 a0001c0001t0005g0145 others(8): Show |
12 | HG00099.hp2 HG00558.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+1269_79+1270dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATA | 8 | a0001c0001t0005g0151 a0001c0001t0007g0016 a0001c0001t0007g0057 others(5): Show |
10 | HG02615.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1267_79+1270dup others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATACAT others(5): Show |
2 | a0001c0001t0007g0002 a0001c0001t0041g0062 |
2 | HG00423.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.79+1244_79+1245ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATA | 8 | a0001c0001t0015g0013 a0001c0001t0015g0135 a0001c0001t0015g0136 others(5): Show |
11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+1265_79+1270dup others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(1): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0002g0015 others(8): Show |
13 | HG01081.hp2 HG01346.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+1263_79+1270dup others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(3): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0065 others(13): Show |
20 | HG00140.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.79+1261_79+1270dup others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(5): Show |
30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0037 others(27): Show |
37 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.79+1259_79+1270dup others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(7): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0033 others(16): Show |
25 | HG00280.hp2 HG00544.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+1257_79+1270dup others(14): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(9): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0074 others(3): Show |
8 | HG00609.hp2 HG02145.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+1255_79+1270dup others(16): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0033 |
3 | NA18942.hp1 NA18952.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.79+1253_79+1270dup others(18): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(13): Show |
1 | a0001c0001t0010g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+1251_79+1270dup others(20): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0002 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.79+1247_79+1270dup others(24): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTGTATA | 4 | a0001c0001t0057g0048 a0001c0001t0059g0175 a0001c0001t0068g0177 others(1): Show |
4 | HG03225.hp1 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(6): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTGTATAT others(1): Show |
3 | a0001c0001t0048g0126 a0001c0001t0076g0049 a0001c0001t0103g0171 |
3 | HG01123.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTGTATAT others(3): Show |
3 | a0001c0001t0001g0070 a0001c0001t0010g0032 a0001c0001t0058g0048 |
3 | HG03195.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.79+1241_79+1242ins others(10): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0010g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+1241_79+1242ins others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | GTA | G | 75 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(72): Show |
118 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.79+1269_79+1270del others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645415 | GTATA | G | 7 | a0001c0001t0005g0146 a0001c0001t0063g0012 a0003c0003t0007g0011 others(4): Show |
7 | HG00642.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1267_79+1270del others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645415 | ||||||
chr19:44645417 | A | G | 2 | a0001c0001t0008g0173 a0001c0001t0019g0174 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1242A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645417 | |||||||
chr19:44645419 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0009 |
2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.79+1244A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645419 | |||||||
chr19:44645421 | A | G | 1 | a0001c0001t0003g0001 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79+1246A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645421 | |||||||
chr19:44645443 | A | ATATATAT others(6): Show |
1 | a0001c0001t0024g0036 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.79+1270_79+1271ins others(13): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645443 | ||||||
chr19:44645443 | A | ATATATAT others(8): Show |
3 | a0001c0001t0023g0095 a0001c0001t0023g0096 a0001c0001t0024g0094 |
3 | HG00741.hp1 HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.79+1270_79+1271ins others(15): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645443 | ||||||
chr19:44645456 | G | T | 4 | a0001c0001t0023g0095 a0001c0001t0023g0096 a0001c0001t0024g0036 others(1): Show |
5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1281G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645456 | |||||||
chr19:44645458 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.79+1283G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645458 | |||||||
chr19:44645477 | T | TGAGA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(133): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.79+1307_79+1310dup others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44645477 | ||||||
chr19:44645671 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(68): Show |
103 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+1496C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645671 | |||||||
chr19:44645742 | C | T | 1 | a0003c0003t0109g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-1481C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645742 | |||||||
chr19:44645842 | A | G | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-1381A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645842 | |||||||
chr19:44645964 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(133): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.80-1259G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44645964 | |||||||
chr19:44646144 | C | A | 1 | a0002c0002t0083g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.80-1079C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646144 | |||||||
chr19:44646217 | AC | A | 2 | a0001c0001t0002g0015 a0001c0001t0005g0015 |
5 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1004delC | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44646217 | ||||||
chr19:44646220 | G | A | 1 | a0001c0001t0008g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.80-1003G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646220 | |||||||
chr19:44646342 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(273): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.80-881T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646342 | |||||||
chr19:44646377 | G | A | 3 | a0006c0007t0029g0125 a0006c0007t0056g0042 a0006c0012t0029g0042 |
3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.80-846G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646377 | |||||||
chr19:44646456 | C | T | 1 | a0003c0003t0118g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.80-767C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646456 | |||||||
chr19:44646467 | C | A | 2 | a0001c0001t0008g0173 a0001c0001t0019g0174 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80-756C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646467 | |||||||
chr19:44646497 | G | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.80-726G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646497 | |||||||
chr19:44646569 | A | C | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-654A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646569 | |||||||
chr19:44646633 | G | A | 3 | a0006c0007t0029g0125 a0006c0007t0056g0042 a0006c0012t0029g0042 |
3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.80-590G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646633 | |||||||
chr19:44646664 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80-559C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646664 | |||||||
chr19:44646686 | C | G | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.80-537C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646686 | |||||||
chr19:44646698 | A | G | 8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-525A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646698 | |||||||
chr19:44646730 | C | G | 10 | a0001c0001t0008g0173 a0001c0001t0008g0176 a0001c0001t0019g0174 others(7): Show |
10 | HG01123.hp1 HG02109.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-493C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646730 | |||||||
chr19:44646935 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.80-288G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44646935 | |||||||
chr19:44647083 | T | C | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.80-140T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44647083 | |||||||
chr19:44647161 | G | A | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-62G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | chr19 | 44647161 | |||||||
chr19:44647186 | GC | G | 8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-33delC | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 44647186 | ||||||
chr19:44647709 | G | A | 8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.427+139G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44647709 | |||||||
chr19:44647895 | G | T | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.427+325G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44647895 | |||||||
chr19:44648008 | C | A | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.427+438C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648008 | |||||||
chr19:44648013 | T | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0132 a0001c0001t0005g0043 others(4): Show |
9 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+443T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648013 | |||||||
chr19:44648040 | C | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.427+470C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648040 | |||||||
chr19:44648041 | G | A | 1 | a0002c0002t0006g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.427+471G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648041 | |||||||
chr19:44648225 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0097 a0001c0001t0010g0064 |
3 | HG00140.hp2 HG01175.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.427+655T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648225 | |||||||
chr19:44648244 | C | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.427+674C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648244 | |||||||
chr19:44648304 | G | C | 1 | a0001c0001t0007g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.427+734G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648304 | |||||||
chr19:44648484 | A | C | 3 | a0001c0001t0068g0177 a0001c0001t0069g0049 a0001c0001t0076g0049 |
3 | HG03225.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.427+914A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648484 | |||||||
chr19:44648488 | T | C | 1 | a0001c0001t0114g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.427+918T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648488 | |||||||
chr19:44648567 | G | C | 1 | a0002c0002t0019g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.427+997G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648567 | |||||||
chr19:44648593 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | NA18953.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.427+1023G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648593 | |||||||
chr19:44648652 | C | CTGTTT | 53 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(50): Show |
80 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.427+1104_427+1108d others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | ||||||
chr19:44648652 | C | CTGTTTTG others(3): Show |
10 | a0001c0001t0028g0053 a0001c0001t0028g0087 a0001c0001t0040g0023 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.427+1099_427+1108d others(12): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | ||||||
chr19:44648652 | C | CTGTTTTG others(8): Show |
1 | a0002c0002t0085g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+1094_427+1108d others(17): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | ||||||
chr19:44648652 | CTGTTT | C | 8 | a0001c0001t0015g0013 a0001c0001t0015g0135 a0001c0001t0015g0136 others(5): Show |
11 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.427+1104_427+1108d others(7): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44648652 | ||||||
chr19:44648674 | G | C | 10 | a0001c0001t0003g0138 a0001c0001t0015g0013 a0001c0001t0015g0135 others(7): Show |
13 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.427+1104G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648674 | |||||||
chr19:44648679 | C | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(137): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.427+1109C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648679 | |||||||
chr19:44648684 | C | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(129): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.427+1114C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648684 | |||||||
chr19:44648990 | T | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(6): Show |
12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-819T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44648990 | |||||||
chr19:44649122 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(153): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.428-687T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649122 | |||||||
chr19:44649140 | G | A | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.428-669G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649140 | |||||||
chr19:44649247 | A | G | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-562A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649247 | |||||||
chr19:44649316 | G | T | 10 | a0003c0003t0007g0017 a0003c0003t0007g0088 a0003c0003t0007g0089 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-493G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649316 | |||||||
chr19:44649418 | A | G | 9 | a0002c0002t0004g0007 a0002c0002t0004g0040 a0002c0002t0004g0107 others(6): Show |
13 | HG02155.hp1 NA18612.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-391A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649418 | |||||||
chr19:44649427 | C | CT | 128 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0033 others(125): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.428-362dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44649427 | ||||||
chr19:44649427 | C | CTT | 6 | a0001c0001t0001g0020 a0001c0001t0010g0064 a0001c0001t0041g0020 others(3): Show |
7 | HG01175.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-363_428-362dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 44649427 | ||||||
chr19:44649451 | A | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0045 a0001c0001t0002g0155 others(40): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.428-358A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649451 | |||||||
chr19:44649468 | C | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.428-341C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649468 | |||||||
chr19:44649486 | G | A | 2 | a0001c0001t0014g0031 a0001c0001t0031g0031 |
3 | NA19068.hp2 NA19077.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.428-323G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649486 | |||||||
chr19:44649651 | C | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(6): Show |
12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-158C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649651 | |||||||
chr19:44649701 | G | A | 1 | a0001c0001t0009g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.428-108G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649701 | |||||||
chr19:44649712 | C | T | 2 | a0001c0004t0026g0153 a0001c0004t0027g0128 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.428-97C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 2/7 | chr19 | 44649712 | |||||||
chr19:44650157 | C | T | 2 | a0001c0001t0105g0085 a0001c0001t0106g0084 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.724+52C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650157 | |||||||
chr19:44650190 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.724+85G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650190 | |||||||
chr19:44650274 | C | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+169C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650274 | |||||||
chr19:44650283 | C | A | 1 | a0002c0002t0016g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.724+178C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650283 | |||||||
chr19:44650353 | G | C | 2 | a0001c0001t0024g0036 a0001c0001t0024g0094 |
3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.724+248G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650353 | |||||||
chr19:44650530 | A | T | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.724+425A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650530 | |||||||
chr19:44650561 | C | CT | 21 | a0001c0001t0008g0139 a0001c0001t0039g0118 a0001c0001t0040g0023 others(18): Show |
22 | HG00735.hp1 HG00738.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.724+475dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44650561 | ||||||
chr19:44650561 | CT | C | 21 | a0001c0001t0001g0069 a0001c0001t0002g0132 a0001c0001t0002g0155 others(18): Show |
23 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.724+475delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44650561 | ||||||
chr19:44650632 | G | A | 11 | a0001c0001t0002g0018 a0001c0001t0005g0018 a0001c0001t0005g0145 others(8): Show |
17 | HG00438.hp2 HG00609.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.724+527G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650632 | |||||||
chr19:44650860 | C | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+755C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650860 | |||||||
chr19:44650894 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.724+789A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44650894 | |||||||
chr19:44651013 | G | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724+908G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651013 | |||||||
chr19:44651068 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(129): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.724+963G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651068 | |||||||
chr19:44651276 | G | A | 1 | a0001c0001t0005g0146 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.724+1171G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651276 | |||||||
chr19:44651342 | A | G | 4 | a0001c0001t0023g0095 a0001c0001t0023g0096 a0001c0001t0024g0036 others(1): Show |
5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+1237A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651342 | |||||||
chr19:44651466 | G | A | 2 | a0001c0001t0008g0173 a0001c0001t0019g0174 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.724+1361G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651466 | |||||||
chr19:44651843 | C | T | 10 | a0003c0003t0007g0017 a0003c0003t0007g0088 a0003c0003t0007g0089 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+1738C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651843 | |||||||
chr19:44651853 | A | T | 41 | a0002c0002t0003g0038 a0002c0002t0004g0004 a0002c0002t0004g0007 others(38): Show |
64 | HG00140.hp1 HG00642.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.724+1748A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44651853 | |||||||
chr19:44652119 | G | T | 2 | a0001c0001t0002g0015 a0001c0001t0005g0015 |
5 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-1781G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652119 | |||||||
chr19:44652365 | A | ATTTTTG | 10 | a0001c0004t0025g0027 a0001c0004t0025g0129 a0001c0004t0026g0027 others(7): Show |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-1511_725-1506d others(8): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 44652365 | ||||||
chr19:44652443 | G | T | 10 | a0001c0004t0025g0027 a0001c0004t0025g0129 a0001c0004t0026g0027 others(7): Show |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-1457G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652443 | |||||||
chr19:44652506 | C | T | 3 | a0006c0007t0029g0125 a0006c0007t0056g0042 a0006c0012t0029g0042 |
3 | HG02896.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.725-1394C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652506 | |||||||
chr19:44652765 | T | C | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-1135T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652765 | |||||||
chr19:44652771 | T | C | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-1129T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652771 | |||||||
chr19:44652889 | T | C | 1 | a0001c0001t0040g0119 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.725-1011T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652889 | |||||||
chr19:44652891 | A | T | 2 | a0002c0002t0006g0041 a0002c0002t0016g0041 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.725-1009A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44652891 | |||||||
chr19:44653041 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.725-859C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653041 | |||||||
chr19:44653107 | C | T | 8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-793C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653107 | |||||||
chr19:44653108 | G | A | 2 | a0001c0001t0120g0116 a0002c0002t0085g0060 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.725-792G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653108 | |||||||
chr19:44653155 | A | C | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-745A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653155 | |||||||
chr19:44653156 | C | A | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.725-744C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653156 | |||||||
chr19:44653179 | C | T | 1 | a0001c0001t0120g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.725-721C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653179 | |||||||
chr19:44653336 | C | T | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.725-564C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653336 | |||||||
chr19:44653569 | C | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0122 a0001c0001t0005g0015 others(6): Show |
12 | HG01081.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.725-331C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653569 | |||||||
chr19:44653769 | T | G | 2 | a0001c0001t0020g0028 a0001c0001t0033g0028 |
3 | HG01074.hp2 HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.725-131T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653769 | |||||||
chr19:44653790 | G | T | 30 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(27): Show |
32 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.725-110G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653790 | |||||||
chr19:44653809 | C | T | 1 | a0001c0001t0019g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.725-91C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653809 | |||||||
chr19:44653859 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.725-41A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 3/7 | chr19 | 44653859 | |||||||
chr19:44654074 | G | A | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+57G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654074 | |||||||
chr19:44654075 | A | G | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+58A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654075 | |||||||
chr19:44654170 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0010g0032 |
3 | HG03688.hp1 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.842+153C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654170 | |||||||
chr19:44654187 | A | C | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+170A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654187 | |||||||
chr19:44654191 | G | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+174G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654191 | |||||||
chr19:44654199 | G | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+182G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654199 | |||||||
chr19:44654201 | T | C | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+184T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654201 | |||||||
chr19:44654203 | T | C | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+186T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654203 | |||||||
chr19:44654208 | C | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+191C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654208 | |||||||
chr19:44654215 | A | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+198A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654215 | |||||||
chr19:44654221 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(166): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.842+204A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654221 | |||||||
chr19:44654224 | G | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+207G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654224 | |||||||
chr19:44654232 | T | TGG | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+217_842+218dup others(2): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44654232 | ||||||
chr19:44654236 | C | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+219C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654236 | |||||||
chr19:44654236 | CCTGGACC others(31): Show |
C | 77 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(74): Show |
104 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.842+246_842+283del others(38): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44654236 | ||||||
chr19:44654250 | T | A | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+233T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654250 | |||||||
chr19:44654274 | T | C | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+257T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654274 | |||||||
chr19:44654282 | C | G | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+265C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654282 | |||||||
chr19:44654300 | G | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+283G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654300 | |||||||
chr19:44654324 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0132 a0001c0001t0005g0043 others(4): Show |
9 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+307G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654324 | |||||||
chr19:44654544 | G | A | 2 | a0001c0001t0105g0085 a0001c0001t0106g0084 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.842+527G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654544 | |||||||
chr19:44654571 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.842+554C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654571 | |||||||
chr19:44654642 | G | A | 8 | a0001c0001t0002g0045 a0001c0001t0002g0155 a0001c0001t0014g0031 others(5): Show |
9 | HG00423.hp2 HG02080.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+625G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654642 | |||||||
chr19:44654737 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.842+720T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654737 | |||||||
chr19:44654770 | T | C | 82 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(79): Show |
109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+753T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654770 | |||||||
chr19:44654880 | C | G | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+863C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44654880 | |||||||
chr19:44655035 | GATAATAC others(8): Show |
G | 2 | a0001c0001t0028g0053 a0001c0001t0028g0087 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.842+1035_842+1049d others(17): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655035 | ||||||
chr19:44655098 | T | A | 1 | a0001c0001t0002g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.842+1081T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655098 | |||||||
chr19:44655144 | C | T | 82 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(79): Show |
109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+1127C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655144 | |||||||
chr19:44655170 | A | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1153A>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655170 | |||||||
chr19:44655186 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0010g0073 |
2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.842+1169G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655186 | |||||||
chr19:44655228 | G | C | 2 | a0003c0003t0007g0088 a0003c0003t0007g0089 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.842+1211G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655228 | |||||||
chr19:44655380 | C | T | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+1363C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655380 | |||||||
chr19:44655382 | C | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1365C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655382 | |||||||
chr19:44655384 | C | A | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1367C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655384 | |||||||
chr19:44655385 | A | G | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1368A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655385 | |||||||
chr19:44655386 | G | A | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1369G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655386 | |||||||
chr19:44655449 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.842+1432T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655449 | |||||||
chr19:44655484 | GT | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(174): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.842+1469delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655484 | ||||||
chr19:44655608 | G | A | 5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+1591G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655608 | |||||||
chr19:44655668 | C | A | 2 | a0001c0001t0038g0019 a0001c0001t0090g0019 |
3 | HG01099.hp1 HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.842+1651C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655668 | |||||||
chr19:44655715 | T | A | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.842+1698T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655715 | |||||||
chr19:44655745 | G | T | 1 | a0001c0001t0003g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.842+1728G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655745 | |||||||
chr19:44655756 | T | C | 82 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(79): Show |
109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.842+1739T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655756 | |||||||
chr19:44655787 | GT | G | 3 | a0001c0001t0057g0048 a0001c0001t0058g0048 a0001c0001t0059g0175 |
3 | HG03195.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.842+1773delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655787 | ||||||
chr19:44655863 | C | CT | 104 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0033 others(101): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.842+1870dupT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | ||||||
chr19:44655863 | C | CTT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0070 others(20): Show |
29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.842+1869_842+1870d others(4): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | ||||||
chr19:44655863 | CT | C | 37 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(34): Show |
41 | HG01109.hp2 HG01257.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.842+1870delT | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44655863 | ||||||
chr19:44655890 | G | C | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.843-1872G>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44655890 | |||||||
chr19:44656338 | G | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0029 a0001c0001t0011g0143 others(2): Show |
9 | HG00438.hp2 HG02165.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1424G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656338 | |||||||
chr19:44656368 | C | A | 82 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(79): Show |
109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.843-1394C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656368 | |||||||
chr19:44656394 | G | A | 4 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0091g0117 others(1): Show |
4 | HG00738.hp1 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1368G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656394 | |||||||
chr19:44656463 | C | A | 1 | a0001c0001t0008g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.843-1299C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656463 | |||||||
chr19:44656522 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.843-1240C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656522 | |||||||
chr19:44656545 | T | C | 1 | a0001c0001t0103g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.843-1217T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656545 | |||||||
chr19:44656577 | A | G | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.843-1185A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656577 | |||||||
chr19:44656668 | C | T | 77 | a0001c0001t0028g0053 a0001c0001t0028g0087 a0001c0001t0039g0115 others(74): Show |
102 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.843-1094C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656668 | |||||||
chr19:44656750 | A | G | 6 | a0003c0003t0007g0017 a0003c0003t0007g0088 a0003c0003t0007g0089 others(3): Show |
7 | HG01109.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1012A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44656750 | |||||||
chr19:44656993 | AATT | A | 82 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(79): Show |
109 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.843-767_843-765del others(3): Show |
PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 44656993 | ||||||
chr19:44657123 | G | A | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-639G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657123 | |||||||
chr19:44657196 | C | G | 1 | a0001c0001t0002g0150 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.843-566C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657196 | |||||||
chr19:44657255 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(57): Show |
90 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.843-507G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657255 | |||||||
chr19:44657507 | C | T | 2 | a0001c0001t0105g0085 a0001c0001t0106g0084 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.843-255C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657507 | |||||||
chr19:44657524 | A | G | 1 | a0002c0002t0016g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.843-238A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657524 | |||||||
chr19:44657614 | A | G | 2 | a0003c0003t0045g0035 a0003c0003t0046g0035 |
2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.843-148A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657614 | |||||||
chr19:44657628 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(156): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.843-134T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657628 | |||||||
chr19:44657696 | G | A | 1 | a0001c0001t0023g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.843-66G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657696 | |||||||
chr19:44657717 | G | A | 5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-45G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 4/7 | chr19 | 44657717 | |||||||
chr19:44657977 | A | C | 1 | a0001c0001t0001g0033 | 2 | NA18942.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.991+67A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44657977 | |||||||
chr19:44658099 | A | G | 1 | a0001c0001t0017g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.991+189A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658099 | |||||||
chr19:44658198 | T | C | 1 | a0002c0002t0004g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.991+288T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658198 | |||||||
chr19:44658199 | T | G | 1 | a0001c0001t0080g0159 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.991+289T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658199 | |||||||
chr19:44658233 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.991+323C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658233 | |||||||
chr19:44658298 | T | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(166): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.991+388T>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658298 | |||||||
chr19:44658490 | A | C | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.992-252A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658490 | |||||||
chr19:44658627 | A | G | 4 | a0001c0001t0023g0095 a0001c0001t0023g0096 a0001c0001t0024g0036 others(1): Show |
5 | HG00741.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-115A>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658627 | |||||||
chr19:44658697 | C | T | 5 | a0001c0001t0040g0023 a0001c0001t0040g0119 a0001c0001t0092g0023 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-45C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 5/7 | chr19 | 44658697 | |||||||
chr19:44658921 | C | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(47): Show |
80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1150+21C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44658921 | |||||||
chr19:44659067 | A | C | 7 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(4): Show |
9 | HG02615.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150+167A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659067 | |||||||
chr19:44659101 | C | T | 5 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+201C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659101 | |||||||
chr19:44659175 | T | C | 1 | a0010c0011t0002g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1150+275T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659175 | |||||||
chr19:44659326 | G | A | 1 | a0001c0001t0114g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1150+426G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659326 | |||||||
chr19:44659396 | G | A | 2 | a0001c0001t0039g0118 a0001c0001t0091g0117 |
2 | HG00738.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1150+496G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659396 | |||||||
chr19:44659399 | C | T | 36 | a0001c0001t0028g0053 a0001c0001t0028g0087 a0001c0001t0039g0115 others(33): Show |
38 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.1150+499C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659399 | |||||||
chr19:44659679 | G | A | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150+779G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659679 | |||||||
chr19:44659687 | G | A | 70 | a0001c0001t0007g0016 a0001c0001t0007g0057 a0001c0001t0007g0058 others(67): Show |
97 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1150+787G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44659687 | |||||||
chr19:44660006 | G | T | 10 | a0003c0003t0007g0017 a0003c0003t0007g0088 a0003c0003t0007g0089 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+1106G>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660006 | |||||||
chr19:44660170 | G | A | 9 | a0001c0001t0039g0115 a0001c0001t0039g0118 a0001c0001t0040g0023 others(6): Show |
9 | HG00738.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151-1122G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660170 | |||||||
chr19:44660183 | C | T | 1 | a0002c0002t0008g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1151-1109C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660183 | |||||||
chr19:44660184 | G | A | 22 | a0001c0001t0048g0126 a0003c0003t0007g0011 a0003c0003t0007g0017 others(19): Show |
24 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1151-1108G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660184 | |||||||
chr19:44660199 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1151-1093G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660199 | |||||||
chr19:44660249 | C | G | 2 | a0001c0001t0002g0132 a0001c0001t0005g0133 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1151-1043C>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660249 | |||||||
chr19:44660404 | T | C | 83 | a0001c0001t0004g0047 a0001c0001t0006g0161 a0001c0001t0007g0016 others(80): Show |
111 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1151-888T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660404 | |||||||
chr19:44660451 | T | C | 5 | a0001c0001t0013g0030 a0001c0001t0013g0123 a0001c0001t0013g0144 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-841T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660451 | |||||||
chr19:44660581 | G | A | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1151-711G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660581 | |||||||
chr19:44660642 | C | T | 2 | a0001c0001t0008g0173 a0001c0001t0019g0174 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1151-650C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660642 | |||||||
chr19:44660673 | C | T | 1 | a0002c0002t0016g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1151-619C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660673 | |||||||
chr19:44660721 | G | A | 1 | a0001c0001t0003g0149 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1151-571G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660721 | |||||||
chr19:44660725 | T | C | 2 | a0001c0001t0002g0148 a0001c0001t0005g0151 |
2 | HG00558.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1151-567T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660725 | |||||||
chr19:44660766 | C | T | 1 | a0002c0002t0006g0108 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1151-526C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660766 | |||||||
chr19:44660831 | G | A | 5 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(2): Show |
5 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-461G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660831 | |||||||
chr19:44660874 | A | C | 1 | a0002c0002t0008g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1151-418A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44660874 | |||||||
chr19:44661029 | T | C | 1 | a0002c0002t0083g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1151-263T>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661029 | |||||||
chr19:44661091 | A | C | 8 | a0001c0001t0008g0176 a0001c0001t0057g0048 a0001c0001t0058g0048 others(5): Show |
8 | HG01123.hp1 HG03130.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-201A>C | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661091 | |||||||
chr19:44661096 | C | T | 1 | a0001c0001t0010g0052 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1151-196C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 6/7 | chr19 | 44661096 | |||||||
chr19:44661349 | G | A | 10 | a0003c0003t0007g0011 a0003c0003t0045g0011 a0003c0003t0045g0035 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182+26G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661349 | |||||||
chr19:44661394 | C | T | 21 | a0003c0003t0007g0011 a0003c0003t0007g0017 a0003c0003t0007g0088 others(18): Show |
23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1182+71C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661394 | |||||||
chr19:44661465 | T | G | 82 | a0001c0001t0004g0047 a0001c0001t0006g0161 a0001c0001t0007g0016 others(79): Show |
110 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.1182+142T>G | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661465 | |||||||
chr19:44661496 | C | T | 2 | a0001c0001t0046g0083 a0001c0001t0114g0086 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1182+173C>T | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661496 | |||||||
chr19:44661497 | G | A | 1 | a0003c0003t0117g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1182+174G>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661497 | |||||||
chr19:44661564 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1183-176C>A | PVR | ENSG00000073008.16 | transcript | ENST00000425690.8 | protein_coding | 7/7 | chr19 | 44661564 |