Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7415 |
| ensemblid | ENSG00000165280.18 |
| hgncid | 12666 |
| symbol | VCP |
| name | valosin containing protein |
| refseq_nuc | NM_007126.5 |
| refseq_prot | NP_009057.1 |
| ensembl_nuc | ENST00000358901.11 |
| ensembl_prot | ENSP00000351777.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 35056064 |
| end | 35072625 |
| strand | - |
| ver | v1.2 |
| region | chr9:35056064-35072625 |
| region5000 | chr9:35051064-35077625 |
| regionname0 | VCP_chr9_35056064_35072625 |
| regionname5000 | VCP_chr9_35051064_35077625 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 806 | 411 | 90 | 74 | 188 | 12 | 45 | 148 | VCP_chr9_35051064_35077625 | VCP | MASGA others(801): Show |
chr9 | 35051064 | 35077625 |
| a0002 | 0/0 | 806 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | MASGA others(801): Show |
chr9 | 35051064 | 35077625 |
| a0003 | 0/0 | 806 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VCP_chr9_35051064_35077625 | VCP | MASGA others(801): Show |
chr9 | 35051064 | 35077625 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2418 | 405 | 89 | 73 | 185 | 12 | 44 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0003 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0004 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0005 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0006 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0007 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0001c0009 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0002c0002 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 | ||
| a0003c0008 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | ATGGC others(2413): Show |
chr9 | 35051064 | 35077625 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3746 | 318 | 61 | 50 | 167 | 8 | 30 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0002 | 0/0 | 3746 | 61 | 16 | 15 | 15 | 3 | 12 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0003 | 0/0 | 3747 | 9 | 9 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3742): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0004 | 0/0 | 3752 | 5 | 2 | 0 | 1 | 1 | 1 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3747): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0005 | 0/0 | 3758 | 4 | 0 | 4 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3753): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0006 | 0/0 | 3746 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0007 | 0/0 | 3746 | 2 | 0 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0009 | 0/0 | 3746 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0010 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0011 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0012 | 0/0 | 3752 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3747): Show |
chr9 | 35051064 | 35077625 |
| a0001c0001t0013 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3759): Show |
chr9 | 35051064 | 35077625 |
| a0001c0003t0001 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0004t0001 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0005t0001 | 0/0 | 3746 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0006t0006 | 0/0 | 3746 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0007t0001 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0001c0009t0001 | 0/0 | 3746 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0002c0002t0008 | 0/0 | 3746 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| a0003c0008t0001 | 0/0 | 3746 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | AGTCT others(3741): Show |
chr9 | 35051064 | 35077625 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 4 | 4 | 28 | 1 | 5 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0002 | 0/0 | 42 | 0 | 1 | 41 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0003 | 0/0 | 17 | 1 | 0 | 15 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 12 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0006 | 0/0 | 12 | 2 | 1 | 9 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0007 | 0/0 | 11 | 1 | 0 | 8 | 0 | 2 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0008 | 0/0 | 11 | 0 | 4 | 0 | 2 | 5 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0009 | 0/0 | 10 | 1 | 4 | 0 | 2 | 3 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0010 | 1/1 | 9 | 6 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0011 | 0/0 | 9 | 5 | 2 | 2 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0012 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0013 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0015 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0017 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0004 | 0/0 | 15 | 1 | 9 | 0 | 0 | 5 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0014 | 0/0 | 7 | 0 | 1 | 2 | 2 | 2 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0003g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0012g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0006t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0001c0009t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0002c0002t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0002c0002t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| a0003c0008t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0071 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0119 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0100 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01261 | hp1 | a0001 | c0006 | t0006 | g0048 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0044 | EUR | IBS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0153 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CDX | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02280 | hp2 | a0002 | c0002 | t0008 | g0154 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0087 | EAS | KHV | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03688 | hp1 | a0001 | c0001 | t0012 | g0150 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03710 | hp1 | a0001 | c0005 | t0001 | g0075 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03834 | hp1 | a0003 | c0008 | t0001 | g0104 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19005 | hp1 | a0001 | c0007 | t0001 | g0103 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19030 | hp1 | a0002 | c0002 | t0008 | g0155 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19076 | hp1 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ASW | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | TSI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02559 | hp1 | a0001 | c0009 | t0001 | g0057 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18955 | hp1 | a0001 | c0004 | t0001 | g0108 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0010 | REF | REF | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | VCP_chr9_35051064_35077625 | VCP | chr9 | 35051064 | 35077625 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:35061172 | T | C | 1 | a0003 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1202A>G | p.Asn401Ser | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 11/17 | 1474/3746 | 1202/2421 | 401/806 | chr9 | 35061172 | |||
| chr9:35068301 | T | C | 1 | a0002 | 2 | HG02280.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.79A>G | p.Ile27Val | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 2/17 | 351/3746 | 79/2421 | 27/806 | chr9 | 35068301 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:35057462 | C | T | 1 | a0001c0004 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.2229G>A | p.Ala743Ala | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 16/17 | 2501/3746 | 2229/2421 | 743/806 | chr9 | 35057462 | |||
| chr9:35057477 | T | C | 1 | a0001c0005 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.2214A>G | p.Glu738Glu | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 16/17 | 2486/3746 | 2214/2421 | 738/806 | chr9 | 35057477 | |||
| chr9:35059793 | T | C | 1 | a0001c0006 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.1704A>G | p.Gln568Gln | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 14/17 | 1976/3746 | 1704/2421 | 568/806 | chr9 | 35059793 | |||
| chr9:35060487 | G | A | 1 | a0001c0007 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1521C>T | p.Gly507Gly | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/17 | 1793/3746 | 1521/2421 | 507/806 | chr9 | 35060487 | |||
| chr9:35062235 | G | A | 1 | a0001c0009 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.927C>T | p.Ile309Ile | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 8/17 | 1199/3746 | 927/2421 | 309/806 | chr9 | 35062235 | |||
| chr9:35068048 | A | G | 1 | a0001c0003 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.145T>C | p.Leu49Leu | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/17 | 417/3746 | 145/2421 | 49/806 | chr9 | 35068048 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:35056077 | A | G | 1 | a0001c0001t0007 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1040T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 1040 | chr9 | 35056077 | ||||||
| chr9:35056081 | G | GT | 1 | a0001c0001t0003 | 9 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1035dupA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 1035 | chr9 | 35056081 | ||||||
| chr9:35056116 | G | A | 2 | a0001c0001t0006 a0001c0006t0006 |
2 | HG01074.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 1001 | chr9 | 35056116 | ||||||
| chr9:35056211 | T | C | 1 | a0001c0001t0009 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*906A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 906 | chr9 | 35056211 | ||||||
| chr9:35056540 | G | A | 1 | a0001c0001t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 577 | chr9 | 35056540 | ||||||
| chr9:35056679 | T | C | 1 | a0001c0001t0012 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 438 | chr9 | 35056679 | ||||||
| chr9:35056964 | C | A | 2 | a0001c0001t0002 a0001c0001t0007 |
63 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*153G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 17/17 | 153 | chr9 | 35056964 | ||||||
| chr9:35072568 | T | C | 1 | a0001c0001t0011 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-215A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/17 | 215 | chr9 | 35072568 | ||||||
| chr9:35072568 | T | TGGCAGC | 2 | a0001c0001t0004 a0001c0001t0012 |
6 | HG00423.hp1 HG01516.hp2 HG01891.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-221_-216dupGCTGCC | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/17 | 216 | chr9 | 35072568 | ||||||
| chr9:35072568 | T | TGGCAGCG others(5): Show |
1 | a0001c0001t0005 | 4 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-227_-216dupGCTGCC others(6): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/17 | 216 | chr9 | 35072568 | ||||||
| chr9:35072568 | T | TGGCAGCG others(11): Show |
1 | a0001c0001t0013 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-233_-216dupGCTGCC others(12): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/17 | 216 | chr9 | 35072568 | ||||||
| chr9:35072620 | G | A | 1 | a0002c0002t0008 | 2 | HG02280.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-267C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/17 | 267 | chr9 | 35072620 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:35057712 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2161-182A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35057712 | |||||||
| chr9:35057750 | T | C | 6 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
8 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.2161-220A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35057750 | |||||||
| chr9:35057771 | G | A | 33 | a0001c0001t0001g0140 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
64 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2161-241C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35057771 | |||||||
| chr9:35057898 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0076 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2161-368T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35057898 | |||||||
| chr9:35057998 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0055 others(2): Show |
9 | HG02622.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2161-468C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35057998 | |||||||
| chr9:35058042 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2161-512C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058042 | |||||||
| chr9:35058172 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2161-642T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058172 | |||||||
| chr9:35058340 | G | T | 1 | a0001c0001t0002g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2160+724C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058340 | |||||||
| chr9:35058341 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2160+723C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058341 | |||||||
| chr9:35058381 | T | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
13 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2160+683A>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058381 | |||||||
| chr9:35058458 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2160+606T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058458 | |||||||
| chr9:35058539 | C | T | 1 | a0001c0005t0001g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2160+525G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058539 | |||||||
| chr9:35058585 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2160+479T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058585 | |||||||
| chr9:35058590 | G | A | 32 | a0001c0001t0001g0140 a0001c0001t0002g0004 a0001c0001t0002g0014 others(29): Show |
63 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2160+474C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058590 | |||||||
| chr9:35058611 | C | G | 32 | a0001c0001t0001g0140 a0001c0001t0002g0004 a0001c0001t0002g0014 others(29): Show |
63 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2160+453G>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058611 | |||||||
| chr9:35058660 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2160+404C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058660 | |||||||
| chr9:35058664 | G | A | 33 | a0001c0001t0001g0140 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
64 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2160+400C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058664 | |||||||
| chr9:35058770 | A | AC | 33 | a0001c0001t0001g0140 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
64 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2160+293_2160+294i others(3): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058770 | |||||||
| chr9:35058777 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2160+287G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058777 | |||||||
| chr9:35058791 | CA | C | 30 | a0001c0001t0001g0102 a0001c0001t0002g0004 a0001c0001t0002g0014 others(27): Show |
59 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2160+272delT | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058791 | |||||||
| chr9:35058793 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2160+271T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058793 | |||||||
| chr9:35058842 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0090 |
6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2160+222A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058842 | |||||||
| chr9:35058887 | G | A | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2160+177C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35058887 | |||||||
| chr9:35059009 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2160+55C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 15/16 | chr9 | 35059009 | |||||||
| chr9:35059272 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2005-53C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 14/16 | chr9 | 35059272 | |||||||
| chr9:35059334 | T | C | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2005-115A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 14/16 | chr9 | 35059334 | |||||||
| chr9:35059345 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2005-126A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 14/16 | chr9 | 35059345 | |||||||
| chr9:35059902 | G | T | 1 | a0001c0001t0003g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1696-101C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35059902 | |||||||
| chr9:35059903 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1696-102A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35059903 | |||||||
| chr9:35059960 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1696-159A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35059960 | |||||||
| chr9:35060024 | C | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0124 others(3): Show |
21 | HG00735.hp1 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1696-223G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35060024 | |||||||
| chr9:35060103 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0042 a0001c0001t0002g0145 |
6 | HG02257.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1695+210G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35060103 | |||||||
| chr9:35060130 | CAA | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1695+181_1695+182d others(4): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35060130 | |||||||
| chr9:35060147 | A | G | 1 | a0001c0001t0002g0029 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1695+166T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35060147 | |||||||
| chr9:35060305 | T | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
splice_region_variant&intron_variant | LOW | c.1695+8A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 13/16 | chr9 | 35060305 | |||||||
| chr9:35060599 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0099 |
3 | HG01168.hp2 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1483-74G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 12/16 | chr9 | 35060599 | |||||||
| chr9:35060749 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1482+52T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 12/16 | chr9 | 35060749 | |||||||
| chr9:35060783 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1482+18A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 12/16 | chr9 | 35060783 | |||||||
| chr9:35060958 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1360-35A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 11/16 | chr9 | 35060958 | |||||||
| chr9:35061419 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1194+158G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 10/16 | chr9 | 35061419 | |||||||
| chr9:35061423 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1194+154G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 10/16 | chr9 | 35061423 | |||||||
| chr9:35061493 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(15): Show |
52 | HG01109.hp2 HG01255.hp1 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.1194+84G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 10/16 | chr9 | 35061493 | |||||||
| chr9:35061506 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(23): Show |
92 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1194+71A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 10/16 | chr9 | 35061506 | |||||||
| chr9:35061696 | G | GACAGTAC others(4): Show |
51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
splice_region_variant&intron_variant | LOW | c.1082-18_1082-8dupT others(10): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 9/16 | chr9 | 35061696 | |||||||
| chr9:35061698 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1082-9G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 9/16 | chr9 | 35061698 | |||||||
| chr9:35061976 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1081+27C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 9/16 | chr9 | 35061976 | |||||||
| chr9:35062616 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.812-266T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 7/16 | chr9 | 35062616 | |||||||
| chr9:35062655 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.812-305A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 7/16 | chr9 | 35062655 | |||||||
| chr9:35062881 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.811+97C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 7/16 | chr9 | 35062881 | |||||||
| chr9:35062882 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.811+96G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 7/16 | chr9 | 35062882 | |||||||
| chr9:35062975 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
splice_region_variant&intron_variant | LOW | c.811+3G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 7/16 | chr9 | 35062975 | |||||||
| chr9:35063342 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.709-262T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063342 | |||||||
| chr9:35063387 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.709-307G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063387 | |||||||
| chr9:35063624 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.708+530T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063624 | |||||||
| chr9:35063625 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.708+529A>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063625 | |||||||
| chr9:35063675 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.708+479G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063675 | |||||||
| chr9:35063704 | T | C | 6 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
8 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+450A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063704 | |||||||
| chr9:35063727 | A | G | 51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+427T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063727 | |||||||
| chr9:35063792 | T | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0125 others(3): Show |
16 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.708+362A>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063792 | |||||||
| chr9:35063940 | G | A | 6 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
8 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+214C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35063940 | |||||||
| chr9:35064099 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.708+55G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 6/16 | chr9 | 35064099 | |||||||
| chr9:35064328 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.577-43T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064328 | |||||||
| chr9:35064334 | G | A | 1 | a0002c0002t0008g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577-49C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064334 | |||||||
| chr9:35064388 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.577-103C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064388 | |||||||
| chr9:35064408 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0074 |
3 | NA18939.hp2 NA18946.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.577-123G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064408 | |||||||
| chr9:35064418 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.577-133C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064418 | |||||||
| chr9:35064551 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.577-266T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064551 | |||||||
| chr9:35064557 | C | A | 2 | a0002c0002t0008g0154 a0002c0002t0008g0155 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577-272G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064557 | |||||||
| chr9:35064577 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.577-292G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064577 | |||||||
| chr9:35064621 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.577-336T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064621 | |||||||
| chr9:35064647 | G | C | 1 | a0001c0001t0001g0024 | 3 | HG02717.hp2 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.577-362C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064647 | |||||||
| chr9:35064748 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.577-463C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064748 | |||||||
| chr9:35064790 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.576+461G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064790 | |||||||
| chr9:35064791 | A | G | 51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.576+460T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35064791 | |||||||
| chr9:35065040 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.576+211C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 5/16 | chr9 | 35065040 | |||||||
| chr9:35065410 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.446-29A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065410 | |||||||
| chr9:35065417 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.446-36C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065417 | |||||||
| chr9:35065521 | C | T | 2 | a0001c0001t0006g0100 a0001c0006t0006g0048 |
2 | HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.446-140G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065521 | |||||||
| chr9:35065683 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.446-302A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065683 | |||||||
| chr9:35065755 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.446-374G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065755 | |||||||
| chr9:35065825 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0143 |
5 | HG01192.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-444G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065825 | |||||||
| chr9:35065982 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0135 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.446-601G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35065982 | |||||||
| chr9:35066125 | C | CA | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(11): Show |
21 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.445+549dupT | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066125 | |||||||
| chr9:35066150 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.445+525T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066150 | |||||||
| chr9:35066159 | G | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0055 others(3): Show |
10 | HG02622.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.445+516C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066159 | |||||||
| chr9:35066264 | CT | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.445+410delA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066264 | |||||||
| chr9:35066267 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.445+408A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066267 | |||||||
| chr9:35066405 | G | A | 1 | a0001c0009t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+270C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066405 | |||||||
| chr9:35066458 | C | A | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
13 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.445+217G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066458 | |||||||
| chr9:35066471 | C | A | 1 | a0001c0001t0002g0129 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.445+204G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066471 | |||||||
| chr9:35066473 | C | G | 1 | a0002c0002t0008g0154 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445+202G>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066473 | |||||||
| chr9:35066571 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.445+104G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066571 | |||||||
| chr9:35066582 | T | TA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.445+92dupT | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066582 | |||||||
| chr9:35066582 | TA | T | 7 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0082 others(4): Show |
8 | HG01109.hp1 HG01168.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+92delT | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 4/16 | chr9 | 35066582 | |||||||
| chr9:35066977 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0097 others(1): Show |
9 | HG01261.hp2 HG01928.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-160C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35066977 | |||||||
| chr9:35067036 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.303-219T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067036 | |||||||
| chr9:35067308 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.303-491C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067308 | |||||||
| chr9:35067457 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.302+434T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067457 | |||||||
| chr9:35067475 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.302+416G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067475 | |||||||
| chr9:35067482 | T | C | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.302+409A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067482 | |||||||
| chr9:35067597 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.302+294C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067597 | |||||||
| chr9:35067604 | T | C | 4 | a0001c0001t0003g0016 a0001c0001t0003g0043 a0001c0001t0003g0054 others(1): Show |
9 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+287A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067604 | |||||||
| chr9:35067634 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0052 |
5 | HG00673.hp1 HG02132.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+257C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067634 | |||||||
| chr9:35067668 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.302+223C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067668 | |||||||
| chr9:35067693 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0055 |
3 | HG02647.hp1 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.302+198C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067693 | |||||||
| chr9:35067735 | A | C | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.302+156T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 3/16 | chr9 | 35067735 | |||||||
| chr9:35068204 | C | T | 29 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0025 others(26): Show |
58 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.129+47G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 2/16 | chr9 | 35068204 | |||||||
| chr9:35068212 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+39T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 2/16 | chr9 | 35068212 | |||||||
| chr9:35068216 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0090 |
6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+35G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 2/16 | chr9 | 35068216 | |||||||
| chr9:35068367 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0055 |
3 | HG02647.hp1 HG02896.hp2 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.18-5T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068367 | |||||||
| chr9:35068571 | G | A | 5 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0005g0045 others(2): Show |
7 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.18-209C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068571 | |||||||
| chr9:35068643 | A | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.18-281T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068643 | |||||||
| chr9:35068840 | TATA | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0090 |
6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-481_18-479delTA others(1): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068840 | |||||||
| chr9:35068879 | T | C | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18-517A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068879 | |||||||
| chr9:35068904 | A | G | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18-542T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068904 | |||||||
| chr9:35068951 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
54 | HG01109.hp2 HG01255.hp1 HG01496.hp2 others(51): Show |
intron_variant | MODIFIER | c.18-589A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35068951 | |||||||
| chr9:35069145 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.18-783G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069145 | |||||||
| chr9:35069158 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18-796T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069158 | |||||||
| chr9:35069338 | C | CA | 3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0090 |
6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-977dupT | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069338 | |||||||
| chr9:35069444 | C | CT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0031 others(15): Show |
31 | HG00673.hp2 HG00738.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.18-1083dupA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.18-1082G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | CT | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 others(32): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.18-1083delA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | CTT | C | 8 | a0001c0001t0001g0055 a0001c0001t0002g0029 a0001c0001t0002g0040 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.18-1084_18-1083del others(2): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.18-1092_18-1083del others(10): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | CTTTTTTT others(4): Show |
C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
143 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.18-1093_18-1083del others(11): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069444 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.18-1094_18-1083del others(12): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069444 | |||||||
| chr9:35069448 | T | A | 2 | a0002c0002t0008g0154 a0002c0002t0008g0155 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.18-1086A>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069448 | |||||||
| chr9:35069458 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.18-1096A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069458 | |||||||
| chr9:35069584 | C | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0118 a0001c0001t0002g0120 others(3): Show |
12 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.18-1222G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069584 | |||||||
| chr9:35069611 | C | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.18-1249G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069611 | |||||||
| chr9:35069611 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.18-1249G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069611 | |||||||
| chr9:35069751 | GCT | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0132 |
4 | NA18612.hp2 NA18991.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-1391_18-1390del others(2): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069751 | |||||||
| chr9:35069899 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.18-1537A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35069899 | |||||||
| chr9:35070084 | A | G | 6 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
8 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.18-1722T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070084 | |||||||
| chr9:35070223 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18-1861C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070223 | |||||||
| chr9:35070397 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.17+1940T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070397 | |||||||
| chr9:35070553 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1784G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070553 | |||||||
| chr9:35070554 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1783G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070554 | |||||||
| chr9:35070556 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1781G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070556 | |||||||
| chr9:35070557 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1780G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070557 | |||||||
| chr9:35070558 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1779T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070558 | |||||||
| chr9:35070559 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1778C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070559 | |||||||
| chr9:35070560 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1777T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070560 | |||||||
| chr9:35070561 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1776C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070561 | |||||||
| chr9:35070565 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1772G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070565 | |||||||
| chr9:35070567 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1770C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070567 | |||||||
| chr9:35070570 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1767T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070570 | |||||||
| chr9:35070573 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1764T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070573 | |||||||
| chr9:35070574 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1763G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070574 | |||||||
| chr9:35070575 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1762T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070575 | |||||||
| chr9:35070577 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1760C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070577 | |||||||
| chr9:35070579 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1758C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070579 | |||||||
| chr9:35070582 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1755G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070582 | |||||||
| chr9:35070583 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1754T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070583 | |||||||
| chr9:35070585 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1752G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070585 | |||||||
| chr9:35070586 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1751T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070586 | |||||||
| chr9:35070594 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1743C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070594 | |||||||
| chr9:35070595 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1742G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070595 | |||||||
| chr9:35070596 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1741G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070596 | |||||||
| chr9:35070598 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1739C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070598 | |||||||
| chr9:35070599 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1738C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070599 | |||||||
| chr9:35070600 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1737G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070600 | |||||||
| chr9:35070602 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17+1735T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070602 | |||||||
| chr9:35070603 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.17+1734G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070603 | |||||||
| chr9:35070729 | C | T | 28 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0025 others(25): Show |
57 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.17+1608G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070729 | |||||||
| chr9:35070772 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.17+1565C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070772 | |||||||
| chr9:35070777 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0097 others(1): Show |
9 | HG01261.hp2 HG01928.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.17+1560G>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070777 | |||||||
| chr9:35070845 | A | T | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17+1492T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35070845 | |||||||
| chr9:35071014 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.17+1323T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071014 | |||||||
| chr9:35071075 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0069 |
3 | HG03139.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.17+1262A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071075 | |||||||
| chr9:35071087 | A | T | 2 | a0002c0002t0008g0154 a0002c0002t0008g0155 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.17+1250T>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071087 | |||||||
| chr9:35071091 | T | A | 1 | a0001c0004t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.17+1246A>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071091 | |||||||
| chr9:35071094 | T | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0025 others(28): Show |
62 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.17+1243A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071094 | |||||||
| chr9:35071142 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.17+1195C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071142 | |||||||
| chr9:35071195 | T | C | 6 | a0001c0001t0004g0044 a0001c0001t0004g0147 a0001c0001t0004g0149 others(3): Show |
8 | HG01168.hp1 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+1142A>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071195 | |||||||
| chr9:35071290 | T | A | 1 | a0001c0001t0001g0002 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.17+1047A>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071290 | |||||||
| chr9:35071293 | G | GT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0034 others(6): Show |
29 | HG01109.hp2 HG01517.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.17+1043dupA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | G | GTT | 11 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0019 others(8): Show |
33 | HG01884.hp1 HG02135.hp2 HG02559.hp1 others(30): Show |
intron_variant | MODIFIER | c.17+1042_17+1043dup others(2): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GT | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(19): Show |
48 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.17+1043delA | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTT | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(20): Show |
75 | HG00558.hp1 HG00673.hp2 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.17+1042_17+1043del others(2): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTTTTT | G | 7 | a0001c0001t0002g0112 a0001c0001t0002g0118 a0001c0001t0002g0120 others(4): Show |
7 | HG01071.hp1 HG02258.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.17+1039_17+1043del others(5): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTTTTTT | G | 23 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0002g0004 others(20): Show |
53 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.17+1038_17+1043del others(6): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTTTTTTT | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
62 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.17+1037_17+1043del others(7): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0003g0016 others(3): Show |
11 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.17+1033_17+1043del others(11): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071293 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0002g0042 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.17+1027_17+1043del others(17): Show |
VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071293 | |||||||
| chr9:35071301 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.17+1036A>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071301 | |||||||
| chr9:35071388 | C | G | 1 | a0001c0001t0003g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.17+949G>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071388 | |||||||
| chr9:35071396 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0145 |
3 | HG02257.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.17+941C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071396 | |||||||
| chr9:35071427 | G | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
11 | HG00673.hp1 HG02027.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.17+910C>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071427 | |||||||
| chr9:35071544 | A | C | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.17+793T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071544 | |||||||
| chr9:35071588 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.17+749T>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071588 | |||||||
| chr9:35071776 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.17+561C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071776 | |||||||
| chr9:35071777 | C | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.17+560G>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071777 | |||||||
| chr9:35071806 | A | C | 5 | a0001c0001t0002g0025 a0001c0001t0002g0047 a0001c0001t0002g0112 others(2): Show |
7 | HG00621.hp2 HG02165.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.17+531T>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071806 | |||||||
| chr9:35071836 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.17+501G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071836 | |||||||
| chr9:35071900 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.17+437G>C | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35071900 | |||||||
| chr9:35072004 | G | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.17+333C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072004 | |||||||
| chr9:35072037 | C | T | 1 | a0001c0001t0002g0029 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.17+300G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072037 | |||||||
| chr9:35072077 | G | C | 1 | a0001c0001t0012g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17+260C>G | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072077 | |||||||
| chr9:35072118 | G | A | 1 | a0001c0001t0003g0043 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.17+219C>T | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072118 | |||||||
| chr9:35072191 | C | T | 1 | a0001c0006t0006g0048 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.17+146G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072191 | |||||||
| chr9:35072265 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.17+72G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072265 | |||||||
| chr9:35072305 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.17+32G>A | VCP | ENSG00000165280.18 | transcript | ENST00000358901.11 | protein_coding | 1/16 | chr9 | 35072305 |