Search by Gene
| geneid | 9404 |
|---|---|
| ensemblid | ENSG00000110031.13 |
| hgncid | 14061 |
| symbol | LPXN |
| name | leupaxin |
| refseq_nuc | NM_004811.3 |
| refseq_prot | NP_004802.1 |
| ensembl_nuc | ENST00000395074.7 |
| ensembl_prot | ENSP00000378512.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 58526871 |
| end | 58575856 |
| strand | - |
| ver | v1.2 |
| region | chr11:58526871-58575856 |
| region5000 | chr11:58521871-58580856 |
| regionname0 | LPXN_chr11_58526871_58575856 |
| regionname5000 | LPXN_chr11_58521871_58580856 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 386 | 309 | 73 | 57 | 139 | 10 | 28 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0002 | 0/0 | 386 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0003 | 0/0 | 386 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0004 | 0/0 | 386 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0005 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0006 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1161 | 174 | 52 | 30 | 71 | 4 | 15 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0002 | 0/0 | 1161 | 130 | 21 | 27 | 64 | 5 | 13 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0003 | 0/0 | 1161 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0004 | 0/0 | 1161 | 5 | 0 | 0 | 4 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0005 | 0/0 | 1161 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0006 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0007 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| c0008 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 668 | 322 | 84 | 59 | 139 | 10 | 28 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0002 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0003 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0004 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0005 | 0/0 | 668 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0006 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| t0007 | 0/0 | 668 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0002 | 0/0 | 14 | 0 | 5 | 8 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0005 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0006 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 174 | 52 | 30 | 71 | 4 | 15 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 130 | 21 | 27 | 64 | 5 | 13 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0005c0006 | a0005 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0006c0008 | a0006 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 170 | 48 | 30 | 71 | 4 | 15 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 128 | 21 | 26 | 63 | 5 | 13 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0002t0007 | a0001 | c0002 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0004c0007t0001 | a0004 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0005c0006t0001 | a0005 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| a0006c0008t0001 | a0006 | c0008 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0004g0084 | a0001 | c0001 | t0004 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0001t0006g0115 | a0001 | c0001 | t0006 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0002 | a0001 | c0002 | t0001 | g0002 | 0/0 | 14 | 0 | 5 | 8 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0003 | a0001 | c0002 | t0001 | g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0006 | a0001 | c0002 | t0001 | g0006 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0013 | a0001 | c0002 | t0001 | g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0014 | a0001 | c0002 | t0001 | g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0025 | a0001 | c0002 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0026 | a0001 | c0002 | t0001 | g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0027 | a0001 | c0002 | t0001 | g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0028 | a0001 | c0002 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0029 | a0001 | c0002 | t0001 | g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0030 | a0001 | c0002 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0031 | a0001 | c0002 | t0001 | g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0032 | a0001 | c0002 | t0001 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0033 | a0001 | c0002 | t0001 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0034 | a0001 | c0002 | t0001 | g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0035 | a0001 | c0002 | t0001 | g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0036 | a0001 | c0002 | t0001 | g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0042 | a0001 | c0002 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0116 | a0001 | c0002 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0141 | a0001 | c0002 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0142 | a0001 | c0002 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0143 | a0001 | c0002 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0144 | a0001 | c0002 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0145 | a0001 | c0002 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0146 | a0001 | c0002 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0147 | a0001 | c0002 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0148 | a0001 | c0002 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0149 | a0001 | c0002 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0150 | a0001 | c0002 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0151 | a0001 | c0002 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0152 | a0001 | c0002 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0153 | a0001 | c0002 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0154 | a0001 | c0002 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0155 | a0001 | c0002 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0156 | a0001 | c0002 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0157 | a0001 | c0002 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0158 | a0001 | c0002 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0159 | a0001 | c0002 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0160 | a0001 | c0002 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0161 | a0001 | c0002 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0162 | a0001 | c0002 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0163 | a0001 | c0002 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0164 | a0001 | c0002 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0165 | a0001 | c0002 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0166 | a0001 | c0002 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0167 | a0001 | c0002 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0168 | a0001 | c0002 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0169 | a0001 | c0002 | t0001 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0170 | a0001 | c0002 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0171 | a0001 | c0002 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0172 | a0001 | c0002 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0173 | a0001 | c0002 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0174 | a0001 | c0002 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0175 | a0001 | c0002 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0176 | a0001 | c0002 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0177 | a0001 | c0002 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0179 | a0001 | c0002 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0181 | a0001 | c0002 | t0001 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0182 | a0001 | c0002 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0183 | a0001 | c0002 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0184 | a0001 | c0002 | t0001 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0185 | a0001 | c0002 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0186 | a0001 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0187 | a0001 | c0002 | t0001 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0188 | a0001 | c0002 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0189 | a0001 | c0002 | t0001 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0190 | a0001 | c0002 | t0001 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0191 | a0001 | c0002 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0192 | a0001 | c0002 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0193 | a0001 | c0002 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0194 | a0001 | c0002 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0195 | a0001 | c0002 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0196 | a0001 | c0002 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0197 | a0001 | c0002 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0199 | a0001 | c0002 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0200 | a0001 | c0002 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0201 | a0001 | c0002 | t0001 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0202 | a0001 | c0002 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0203 | a0001 | c0002 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0204 | a0001 | c0002 | t0001 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0205 | a0001 | c0002 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0206 | a0001 | c0002 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0207 | a0001 | c0002 | t0001 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0208 | a0001 | c0002 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0209 | a0001 | c0002 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0210 | a0001 | c0002 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0001g0212 | a0001 | c0002 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0005g0180 | a0001 | c0002 | t0005 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0002t0007g0236 | a0001 | c0002 | t0007 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0004t0001g0104 | a0001 | c0004 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0004t0001g0105 | a0001 | c0004 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0004t0001g0106 | a0001 | c0004 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0004t0001g0107 | a0001 | c0004 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0001c0004t0001g0114 | a0001 | c0004 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0011 | a0002 | c0003 | t0001 | g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0091 | a0002 | c0003 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0092 | a0002 | c0003 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0093 | a0002 | c0003 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0094 | a0002 | c0003 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0095 | a0002 | c0003 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0096 | a0002 | c0003 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0097 | a0002 | c0003 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0002c0003t0001g0098 | a0002 | c0003 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0003c0005t0001g0020 | a0003 | c0005 | t0001 | g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0003c0005t0001g0111 | a0003 | c0005 | t0001 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0003c0005t0001g0112 | a0003 | c0005 | t0001 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0003c0005t0001g0113 | a0003 | c0005 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0004c0007t0001g0178 | a0004 | c0007 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0005c0006t0001g0139 | a0005 | c0006 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| a0006c0008t0001g0040 | a0006 | c0008 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0171 | EUR | GBR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0104 | EUR | FIN | LPXN_chr11_58521871_58580856 | LPXN |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0160 | EUR | FIN | LPXN_chr11_58521871_58580856 | LPXN |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01106 | hp2 | a0001 | c0002 | t0007 | g0236 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0094 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01496 | hp1 | a0003 | c0005 | t0001 | g0020 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0197 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0209 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02145 | hp2 | a0005 | c0006 | t0001 | g0139 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CDX | LPXN_chr11_58521871_58580856 | LPXN |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | LPXN_chr11_58521871_58580856 | LPXN |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0093 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0095 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0092 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0113 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03486 | hp1 | a0003 | c0005 | t0001 | g0020 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03516 | hp2 | a0006 | c0008 | t0001 | g0040 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN |
| HG03540 | hp1 | a0003 | c0005 | t0001 | g0111 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0096 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | LPXN_chr11_58521871_58580856 | LPXN |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | LPXN_chr11_58521871_58580856 | LPXN |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA18939 | hp1 | a0004 | c0007 | t0001 | g0178 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19005 | hp1 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19005 | hp2 | a0001 | c0002 | t0005 | g0180 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| NA19043 | hp1 | a0003 | c0005 | t0001 | g0112 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0114 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0106 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | LPXN_chr11_58521871_58580856 | LPXN |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ASW | LPXN_chr11_58521871_58580856 | LPXN |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | LPXN_chr11_58521871_58580856 | LPXN |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0140 | REF | REF | LPXN_chr11_58521871_58580856 | LPXN |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58527600
|
G | A | 1 | a0005 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1015C>T | p.Arg339Cys | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 1099/1828 | 1015/1161 | 339/386 | chr11 | 58527600 | ||
| chr11:58527642
|
G | A | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.973C>T | p.Arg325Trp | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 1057/1828 | 973/1161 | 325/386 | chr11 | 58527642 | ||
| chr11:58551078
|
G | A | 1 | a0004 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.473C>T | p.Pro158Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 557/1828 | 473/1161 | 158/386 | chr11 | 58551078 | ||
| chr11:58551109
|
G | T | 1 | a0002 | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
missense_variant | MODERATE | c.442C>A | p.Pro148Thr | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 526/1828 | 442/1161 | 148/386 | chr11 | 58551109 | ||
| chr11:58570647
|
G | A | 1 | a0003 | 5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.80C>T | p.Pro27Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/9 | 164/1828 | 80/1161 | 27/386 | chr11 | 58570647 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58550126
|
T | C | 1 | a0001c0004 | 5 | HG00280.hp1 NA19005.hp1 NA19056.hp2 others(2): Show |
synonymous_variant | LOW | c.507A>G | p.Gln169Gln | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 6/9 | 591/1828 | 507/1161 | 169/386 | chr11 | 58550126 | ||
| chr11:58551146
|
C | G | 3 | a0001c0002a0004c0007a0005c0006 | 132 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
synonymous_variant | LOW | c.405G>C | p.Leu135Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 489/1828 | 405/1161 | 135/386 | chr11 | 58551146 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58526960
|
T | A | 1 | a0001c0001t0003 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 494 | chr11 | 58526960 | |||||
| chr11:58527107
|
T | C | 1 | a0001c0001t0004 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 347 | chr11 | 58527107 | |||||
| chr11:58527118
|
A | G | 1 | a0001c0001t0002 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 336 | chr11 | 58527118 | |||||
| chr11:58527202
|
G | A | 1 | a0001c0002t0005 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 252 | chr11 | 58527202 | |||||
| chr11:58527274
|
T | G | 1 | a0001c0001t0006 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 180 | chr11 | 58527274 | |||||
| chr11:58575851
|
G | C | 1 | a0001c0002t0007 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/9 | 79 | chr11 | 58575851 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58527798
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.892-75G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527798 | ||||||
| chr11:58527806
|
T | A | 1 | a0001c0002t0001g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.892-83A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527806 | ||||||
| chr11:58527819
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.892-96G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527819 | ||||||
| chr11:58527831
|
A | G | 1 | a0001c0002t0001g0162 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.892-108T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527831 | ||||||
| chr11:58527874
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(7): Show | 12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.892-151G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527874 | ||||||
| chr11:58527962
|
T | G | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.891+81A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527962 | ||||||
| chr11:58528216
|
A | G | 1 | a0006c0008t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.743-25T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528216 | ||||||
| chr11:58528275
|
TCA | T | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-86_743-85delTG | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528275 | ||||||
| chr11:58528427
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-236C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528427 | ||||||
| chr11:58528551
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.743-360G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528551 | ||||||
| chr11:58528603
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.743-412A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528603 | ||||||
| chr11:58528625
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-434A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528625 | ||||||
| chr11:58528644
|
T | G | 1 | a0001c0002t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.743-453A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528644 | ||||||
| chr11:58528748
|
A | C | 1 | a0001c0002t0001g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.743-557T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528748 | ||||||
| chr11:58528786
|
T | C | 1 | a0003c0005t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.743-595A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528786 | ||||||
| chr11:58528805
|
C | CATATATT others(3): Show |
2 | a0001c0002t0001g0152a0001c0002t0001g0177 | 2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.743-624_743-615dup others(10): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528805 | ||||||
| chr11:58528987
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.743-796A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528987 | ||||||
| chr11:58529126
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-935T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529126 | ||||||
| chr11:58529129
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-938T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529129 | ||||||
| chr11:58529333
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.743-1142C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529333 | ||||||
| chr11:58529384
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0090 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.743-1193C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529384 | ||||||
| chr11:58529437
|
C | T | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.743-1246G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529437 | ||||||
| chr11:58529458
|
A | G | 1 | a0003c0005t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743-1267T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529458 | ||||||
| chr11:58529564
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.743-1373G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529564 | ||||||
| chr11:58529607
|
CA | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(65): Show | 91 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.743-1417delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529607 | ||||||
| chr11:58529634
|
T | A | 1 | a0002c0003t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743-1443A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529634 | ||||||
| chr11:58530069
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-1878G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530069 | ||||||
| chr11:58530253
|
C | T | 1 | a0001c0004t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.743-2062G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530253 | ||||||
| chr11:58530295
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743-2104G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530295 | ||||||
| chr11:58530512
|
G | C | 5 | a0001c0004t0001g0104a0001c0004t0001g0105a0001c0004t0001g0106others(2): Show | 5 | HG00280.hp1 NA19005.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-2321C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530512 | ||||||
| chr11:58530596
|
C | T | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-2405G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530596 | ||||||
| chr11:58530996
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-2805C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530996 | ||||||
| chr11:58531017
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.743-2826C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531017 | ||||||
| chr11:58531043
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.743-2852A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531043 | ||||||
| chr11:58531149
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-2958G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531149 | ||||||
| chr11:58531215
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-3024A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531215 | ||||||
| chr11:58531256
|
G | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0214a0001c0001t0001g0218others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-3065C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531256 | ||||||
| chr11:58531271
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-3080C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531271 | ||||||
| chr11:58531350
|
G | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3159C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531350 | ||||||
| chr11:58531419
|
A | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3228T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531419 | ||||||
| chr11:58531576
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.743-3385C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531576 | ||||||
| chr11:58531613
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-3422T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531613 | ||||||
| chr11:58531626
|
AAC | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0043others(11): Show | 21 | HG01981.hp1 HG02056.hp2 NA18747.hp1 others(18): Show |
intron_variant | MODIFIER | c.743-3437_743-3436d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531626 | ||||||
| chr11:58531660
|
T | A | 3 | a0001c0002t0001g0013a0001c0002t0001g0028a0001c0002t0001g0206 | 6 | HG00558.hp1 HG02040.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3469A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531660 | ||||||
| chr11:58531732
|
G | A | 3 | a0001c0002t0001g0013a0001c0002t0001g0028a0001c0002t0001g0206 | 6 | HG00558.hp1 HG02040.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3541C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531732 | ||||||
| chr11:58531893
|
A | G | 6 | a0001c0002t0001g0034a0001c0002t0001g0036a0001c0002t0001g0201others(3): Show | 8 | HG00741.hp2 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-3702T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531893 | ||||||
| chr11:58531999
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.743-3808T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531999 | ||||||
| chr11:58532000
|
C | G | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-3809G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532000 | ||||||
| chr11:58532021
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.743-3830A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532021 | ||||||
| chr11:58532033
|
G | A | 3 | a0002c0003t0001g0092a0002c0003t0001g0093a0002c0003t0001g0094 | 3 | HG01261.hp2 HG02257.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.743-3842C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532033 | ||||||
| chr11:58532047
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0070others(4): Show | 9 | HG00741.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-3856G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532047 | ||||||
| chr11:58532057
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.743-3866G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532057 | ||||||
| chr11:58532154
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-3963C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532154 | ||||||
| chr11:58532173
|
G | A | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.743-3982C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532173 | ||||||
| chr11:58532188
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3997G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532188 | ||||||
| chr11:58532226
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.743-4035G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532226 | ||||||
| chr11:58532284
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-4093C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532284 | ||||||
| chr11:58532294
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-4103C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532294 | ||||||
| chr11:58532305
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-4114G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532305 | ||||||
| chr11:58532334
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.743-4143C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532334 | ||||||
| chr11:58532357
|
C | T | 2 | a0001c0002t0001g0168a0001c0002t0001g0174 | 2 | NA18969.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.743-4166G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532357 | ||||||
| chr11:58532361
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0044a0003c0005t0001g0020others(4): Show | 8 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-4170G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532361 | ||||||
| chr11:58532362
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.743-4171C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532362 | ||||||
| chr11:58532433
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-4242A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532433 | ||||||
| chr11:58532476
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.743-4285C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532476 | ||||||
| chr11:58532689
|
C | G | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-4498G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532689 | ||||||
| chr11:58532875
|
T | C | 1 | a0001c0001t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.743-4684A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532875 | ||||||
| chr11:58532881
|
T | C | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-4690A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532881 | ||||||
| chr11:58532887
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.743-4696A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532887 | ||||||
| chr11:58532890
|
G | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-4699C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532890 | ||||||
| chr11:58532921
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-4730G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532921 | ||||||
| chr11:58532946
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-4755C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532946 | ||||||
| chr11:58533045
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-4854C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533045 | ||||||
| chr11:58533125
|
AT | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0004g0084 | 3 | HG02622.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.743-4935delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533125 | ||||||
| chr11:58533143
|
C | T | 2 | a0001c0001t0001g0088a0001c0002t0001g0142 | 2 | HG01257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.743-4952G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533143 | ||||||
| chr11:58533204
|
A | T | 1 | a0002c0003t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.743-5013T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533204 | ||||||
| chr11:58533216
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.743-5025G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533216 | ||||||
| chr11:58533233
|
C | T | 3 | a0001c0002t0001g0162a0001c0002t0001g0176a0001c0002t0001g0194 | 3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.743-5042G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533233 | ||||||
| chr11:58533281
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.743-5090A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533281 | ||||||
| chr11:58533320
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.743-5129C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533320 | ||||||
| chr11:58533381
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.743-5190T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533381 | ||||||
| chr11:58533417
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.743-5226T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533417 | ||||||
| chr11:58533494
|
C | T | 1 | a0001c0002t0001g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.743-5303G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533494 | ||||||
| chr11:58533634
|
C | T | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.743-5443G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533634 | ||||||
| chr11:58533767
|
T | C | 4 | a0003c0005t0001g0020a0003c0005t0001g0111a0003c0005t0001g0112others(1): Show | 5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-5576A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533767 | ||||||
| chr11:58533942
|
G | A | 7 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148others(4): Show | 7 | HG00609.hp1 HG00621.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-5751C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533942 | ||||||
| chr11:58534072
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.743-5881C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534072 | ||||||
| chr11:58534193
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.743-6002G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534193 | ||||||
| chr11:58534341
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-6150T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534341 | ||||||
| chr11:58534382
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 44 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.743-6191C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534382 | ||||||
| chr11:58534413
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0196 | 6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-6222G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534413 | ||||||
| chr11:58534463
|
A | G | 3 | a0001c0002t0001g0162a0001c0002t0001g0176a0001c0002t0001g0194 | 3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.743-6272T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534463 | ||||||
| chr11:58534503
|
C | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-6312G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534503 | ||||||
| chr11:58534625
|
G | C | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-6434C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534625 | ||||||
| chr11:58534729
|
C | T | 7 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148others(4): Show | 7 | HG00609.hp1 HG00621.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-6538G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534729 | ||||||
| chr11:58534778
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-6587G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534778 | ||||||
| chr11:58534833
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-6642C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534833 | ||||||
| chr11:58535086
|
G | A | 1 | a0006c0008t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.743-6895C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535086 | ||||||
| chr11:58535270
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.743-7079G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535270 | ||||||
| chr11:58535305
|
T | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-7114A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535305 | ||||||
| chr11:58535324
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.743-7133G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535324 | ||||||
| chr11:58535359
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-7168C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535359 | ||||||
| chr11:58535665
|
G | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-7474C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535665 | ||||||
| chr11:58535667
|
T | C | 2 | a0003c0005t0001g0111a0003c0005t0001g0112 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.743-7476A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535667 | ||||||
| chr11:58535751
|
G | T | 1 | a0001c0002t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.743-7560C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535751 | ||||||
| chr11:58535782
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.743-7591T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535782 | ||||||
| chr11:58535925
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.743-7734A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535925 | ||||||
| chr11:58535988
|
CACTGTTC others(11): Show |
C | 1 | a0001c0002t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.743-7815_743-7798d others(20): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535988 | ||||||
| chr11:58536117
|
T | A | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.743-7926A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536117 | ||||||
| chr11:58536439
|
G | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.743-8248C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536439 | ||||||
| chr11:58536484
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0150a0001c0002t0001g0152 | 3 | HG03831.hp2 NA18942.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.743-8293G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536484 | ||||||
| chr11:58536553
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-8362A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536553 | ||||||
| chr11:58536882
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.743-8691T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536882 | ||||||
| chr11:58536918
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.743-8727G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536918 | ||||||
| chr11:58536987
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0118a0001c0001t0001g0133 | 4 | NA18943.hp2 NA18961.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-8796G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536987 | ||||||
| chr11:58537092
|
AG | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-8902delC | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537092 | ||||||
| chr11:58537307
|
T | C | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.743-9116A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537307 | ||||||
| chr11:58537337
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.743-9146T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537337 | ||||||
| chr11:58537422
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-9231T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537422 | ||||||
| chr11:58537442
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-9251T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537442 | ||||||
| chr11:58537887
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-9696C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537887 | ||||||
| chr11:58537942
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-9751A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537942 | ||||||
| chr11:58537945
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-9754G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537945 | ||||||
| chr11:58538041
|
C | A | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.743-9850G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538041 | ||||||
| chr11:58538077
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-9886G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538077 | ||||||
| chr11:58538333
|
C | A | 4 | a0003c0005t0001g0020a0003c0005t0001g0111a0003c0005t0001g0112others(1): Show | 5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-10142G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538333 | ||||||
| chr11:58538524
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.743-10333A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538524 | ||||||
| chr11:58538783
|
CA | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(16): Show | 25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.743-10593delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538783 | ||||||
| chr11:58539002
|
A | AAAC | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.742+10781_742+1078 others(7): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539002 | ||||||
| chr11:58539002
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.742+10784T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539002 | ||||||
| chr11:58539105
|
G | A | 2 | a0001c0002t0001g0036a0001c0002t0001g0204 | 3 | HG01099.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.742+10681C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539105 | ||||||
| chr11:58539399
|
G | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+10387C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539399 | ||||||
| chr11:58539529
|
A | C | 1 | a0001c0002t0001g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.742+10257T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539529 | ||||||
| chr11:58539570
|
T | C | 2 | a0001c0004t0001g0106a0001c0004t0001g0114 | 2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.742+10216A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539570 | ||||||
| chr11:58539793
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117 | 5 | HG00438.hp1 HG02071.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+9993A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539793 | ||||||
| chr11:58539928
|
A | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9858T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539928 | ||||||
| chr11:58540051
|
C | G | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.742+9735G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540051 | ||||||
| chr11:58540097
|
A | G | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9689T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540097 | ||||||
| chr11:58540161
|
A | C | 7 | a0001c0002t0001g0014a0001c0002t0001g0033a0001c0002t0001g0189others(4): Show | 10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+9625T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540161 | ||||||
| chr11:58540186
|
T | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.742+9600A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540186 | ||||||
| chr11:58540490
|
A | G | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9296T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540490 | ||||||
| chr11:58540495
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9291C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540495 | ||||||
| chr11:58540537
|
C | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9249G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540537 | ||||||
| chr11:58540672
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.742+9114A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540672 | ||||||
| chr11:58540819
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0223 | 2 | NA18988.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.742+8967C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540819 | ||||||
| chr11:58540868
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.742+8918A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540868 | ||||||
| chr11:58540869
|
G | A | 1 | a0006c0008t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+8917C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540869 | ||||||
| chr11:58541048
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+8738A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541048 | ||||||
| chr11:58541085
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742+8701G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541085 | ||||||
| chr11:58541255
|
T | C | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742+8531A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541255 | ||||||
| chr11:58541363
|
T | C | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+8423A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541363 | ||||||
| chr11:58541375
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.742+8411G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541375 | ||||||
| chr11:58541484
|
A | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+8302T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541484 | ||||||
| chr11:58541550
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.742+8236C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541550 | ||||||
| chr11:58541565
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742+8221T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541565 | ||||||
| chr11:58541709
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.742+8077G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541709 | ||||||
| chr11:58541741
|
G | A | 3 | a0001c0002t0001g0162a0001c0002t0001g0176a0001c0002t0001g0194 | 3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.742+8045C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541741 | ||||||
| chr11:58541753
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+8033A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541753 | ||||||
| chr11:58541845
|
A | G | 1 | a0001c0002t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742+7941T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541845 | ||||||
| chr11:58541870
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+7916C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541870 | ||||||
| chr11:58541879
|
T | C | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+7907A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541879 | ||||||
| chr11:58541972
|
T | C | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+7814A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541972 | ||||||
| chr11:58542018
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.742+7768G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542018 | ||||||
| chr11:58542031
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+7755C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542031 | ||||||
| chr11:58542150
|
C | G | 1 | a0001c0004t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742+7636G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542150 | ||||||
| chr11:58542159
|
G | C | 1 | a0001c0002t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.742+7627C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542159 | ||||||
| chr11:58542235
|
T | C | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+7551A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542235 | ||||||
| chr11:58542237
|
A | ATGAG | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+7548_742+7549i others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542237 | ||||||
| chr11:58542350
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.742+7436G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542350 | ||||||
| chr11:58542441
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 178 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.742+7345G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542441 | ||||||
| chr11:58542543
|
A | G | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742+7243T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542543 | ||||||
| chr11:58543017
|
C | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0196 | 6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+6769G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543017 | ||||||
| chr11:58543114
|
C | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.742+6672G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543114 | ||||||
| chr11:58543132
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.742+6654C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543132 | ||||||
| chr11:58543404
|
C | T | 7 | a0001c0002t0001g0014a0001c0002t0001g0033a0001c0002t0001g0189others(4): Show | 10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+6382G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543404 | ||||||
| chr11:58543576
|
C | T | 1 | a0006c0008t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+6210G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543576 | ||||||
| chr11:58543689
|
C | T | 4 | a0003c0005t0001g0020a0003c0005t0001g0111a0003c0005t0001g0112others(1): Show | 5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+6097G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543689 | ||||||
| chr11:58543689
|
CT | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.742+6096delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543689 | ||||||
| chr11:58543720
|
C | A | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742+6066G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543720 | ||||||
| chr11:58543752
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.742+6034T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543752 | ||||||
| chr11:58543832
|
T | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0234 | 2 | HG01192.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.742+5954A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543832 | ||||||
| chr11:58543873
|
T | C | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742+5913A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543873 | ||||||
| chr11:58543895
|
G | T | 1 | a0001c0002t0001g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.742+5891C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543895 | ||||||
| chr11:58543933
|
A | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.742+5853T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543933 | ||||||
| chr11:58544105
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.742+5681G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544105 | ||||||
| chr11:58544442
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.742+5344C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544442 | ||||||
| chr11:58544544
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.742+5242C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544544 | ||||||
| chr11:58544645
|
A | C | 5 | a0002c0003t0001g0011a0002c0003t0001g0092a0002c0003t0001g0093others(2): Show | 7 | HG01261.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+5141T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544645 | ||||||
| chr11:58544726
|
A | C | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+5060T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544726 | ||||||
| chr11:58544845
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742+4941C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544845 | ||||||
| chr11:58544893
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.742+4893C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544893 | ||||||
| chr11:58544921
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.742+4865C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544921 | ||||||
| chr11:58545102
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.742+4684G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545102 | ||||||
| chr11:58545383
|
A | G | 1 | a0002c0003t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.742+4403T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545383 | ||||||
| chr11:58545407
|
C | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.742+4379G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545407 | ||||||
| chr11:58545605
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0065others(1): Show | 4 | HG01934.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+4181A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545605 | ||||||
| chr11:58545606
|
A | G | 1 | a0001c0002t0001g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.742+4180T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545606 | ||||||
| chr11:58545712
|
A | G | 1 | a0001c0001t0001g0007 | 4 | NA18939.hp2 NA18968.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+4074T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545712 | ||||||
| chr11:58545838
|
C | A | 1 | a0001c0002t0001g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.742+3948G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545838 | ||||||
| chr11:58545949
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.742+3837A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545949 | ||||||
| chr11:58546234
|
C | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+3552G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546234 | ||||||
| chr11:58546375
|
CT | C | 4 | a0001c0002t0001g0142a0001c0002t0001g0160a0001c0002t0001g0188others(1): Show | 4 | HG00280.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+3410delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546375 | ||||||
| chr11:58546395
|
A | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+3391T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546395 | ||||||
| chr11:58546953
|
G | T | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+2833C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546953 | ||||||
| chr11:58546970
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+2816G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546970 | ||||||
| chr11:58547067
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.742+2719C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547067 | ||||||
| chr11:58547360
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+2426G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547360 | ||||||
| chr11:58547361
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+2425A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547361 | ||||||
| chr11:58548233
|
T | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+1553A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548233 | ||||||
| chr11:58548260
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02300.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.742+1526A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548260 | ||||||
| chr11:58548342
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.742+1444T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548342 | ||||||
| chr11:58548346
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.742+1440T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548346 | ||||||
| chr11:58548454
|
A | G | 7 | a0001c0002t0001g0014a0001c0002t0001g0033a0001c0002t0001g0189others(4): Show | 10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+1332T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548454 | ||||||
| chr11:58548623
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742+1163G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548623 | ||||||
| chr11:58548734
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.742+1052G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548734 | ||||||
| chr11:58548869
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.742+917C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548869 | ||||||
| chr11:58548902
|
C | T | 1 | a0001c0002t0001g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.742+884G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548902 | ||||||
| chr11:58548909
|
AC | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+876delG | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548909 | ||||||
| chr11:58548930
|
T | C | 1 | a0001c0004t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.742+856A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548930 | ||||||
| chr11:58548961
|
A | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.742+825T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548961 | ||||||
| chr11:58548992
|
G | A | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+794C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548992 | ||||||
| chr11:58549001
|
ATAACATT others(10): Show |
A | 1 | a0001c0002t0001g0165 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.742+768_742+784del others(17): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549001 | ||||||
| chr11:58549094
|
T | C | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+692A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549094 | ||||||
| chr11:58549361
|
G | A | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+425C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549361 | ||||||
| chr11:58549429
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.742+357G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549429 | ||||||
| chr11:58549470
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+316A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549470 | ||||||
| chr11:58549643
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.742+143C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549643 | ||||||
| chr11:58549681
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.742+105A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549681 | ||||||
| chr11:58550175
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.487-29C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550175 | ||||||
| chr11:58550583
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.487-437A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550583 | ||||||
| chr11:58550600
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487-454C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550600 | ||||||
| chr11:58550973
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.486+92T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550973 | ||||||
| chr11:58550992
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+73C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550992 | ||||||
| chr11:58551033
|
G | GGCTGTAG others(9): Show |
1 | a0001c0002t0001g0165 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.486+16_486+31dupAT others(14): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58551033 | ||||||
| chr11:58551538
|
A | T | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-306T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551538 | ||||||
| chr11:58551572
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0074 | 3 | HG02683.hp1 HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.319-340C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551572 | ||||||
| chr11:58551685
|
T | C | 1 | a0001c0002t0001g0150 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.319-453A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551685 | ||||||
| chr11:58551768
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.319-536G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551768 | ||||||
| chr11:58551895
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.319-663T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551895 | ||||||
| chr11:58551911
|
G | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0198 | 3 | HG01167.hp2 HG01169.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.319-679C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551911 | ||||||
| chr11:58552164
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.319-932C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552164 | ||||||
| chr11:58552272
|
C | G | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.319-1040G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552272 | ||||||
| chr11:58552318
|
GA | G | 13 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0135others(10): Show | 15 | HG01496.hp1 HG01978.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.319-1087delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552318 | ||||||
| chr11:58552396
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.319-1164C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552396 | ||||||
| chr11:58552541
|
T | C | 1 | a0001c0002t0005g0180 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.319-1309A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552541 | ||||||
| chr11:58552727
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.319-1495A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552727 | ||||||
| chr11:58552871
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.319-1639G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552871 | ||||||
| chr11:58552883
|
C | T | 1 | a0001c0002t0001g0033 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.319-1651G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552883 | ||||||
| chr11:58552886
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-1654C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552886 | ||||||
| chr11:58553319
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+1522C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553319 | ||||||
| chr11:58553335
|
C | CA | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 139 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.318+1505dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553335 | ||||||
| chr11:58553335
|
CA | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0102a0001c0001t0001g0108others(8): Show | 11 | HG01167.hp2 HG01258.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.318+1505delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553335 | ||||||
| chr11:58553361
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.318+1480C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553361 | ||||||
| chr11:58553405
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.318+1436A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553405 | ||||||
| chr11:58553690
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0085 | 4 | HG02280.hp1 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1151A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553690 | ||||||
| chr11:58553976
|
T | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0043others(11): Show | 21 | HG01981.hp1 HG02056.hp2 NA18747.hp1 others(18): Show |
intron_variant | MODIFIER | c.318+865A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553976 | ||||||
| chr11:58554033
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+808G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554033 | ||||||
| chr11:58554078
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+763C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554078 | ||||||
| chr11:58554228
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0231 | 7 | HG02280.hp2 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+613C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554228 | ||||||
| chr11:58554230
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.318+611A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554230 | ||||||
| chr11:58554317
|
A | T | 1 | a0001c0001t0001g0039 | 2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.318+524T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554317 | ||||||
| chr11:58554797
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.318+44C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554797 | ||||||
| chr11:58555058
|
A | G | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-118T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555058 | ||||||
| chr11:58555313
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219-373C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555313 | ||||||
| chr11:58555594
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.219-654A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555594 | ||||||
| chr11:58555739
|
A | AAC | 27 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(24): Show | 46 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.219-801_219-800dup others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555739 | ||||||
| chr11:58555739
|
A | AACAC | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-803_219-800dup others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555739 | ||||||
| chr11:58555768
|
G | GCA | 15 | a0001c0001t0001g0009a0001c0001t0001g0214a0001c0001t0001g0218others(12): Show | 20 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-830_219-829dup others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | ||||||
| chr11:58555768
|
GCA | G | 101 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0081others(98): Show | 143 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.219-830_219-829del others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | ||||||
| chr11:58555768
|
GCACA | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.219-832_219-829del others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | ||||||
| chr11:58555883
|
A | C | 1 | a0001c0001t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219-943T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555883 | ||||||
| chr11:58555976
|
A | G | 4 | a0001c0002t0001g0164a0001c0002t0001g0165a0001c0002t0001g0166others(1): Show | 4 | HG00438.hp2 NA18975.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-1036T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555976 | ||||||
| chr11:58555994
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(26): Show | 42 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.219-1054A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555994 | ||||||
| chr11:58556100
|
C | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-1160G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556100 | ||||||
| chr11:58556158
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-1218T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556158 | ||||||
| chr11:58556205
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.219-1265G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556205 | ||||||
| chr11:58556261
|
A | G | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.219-1321T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556261 | ||||||
| chr11:58556372
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.219-1432A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556372 | ||||||
| chr11:58556627
|
T | C | 1 | a0003c0005t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-1687A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556627 | ||||||
| chr11:58556798
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.219-1858T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556798 | ||||||
| chr11:58556888
|
G | C | 1 | a0001c0002t0001g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.219-1948C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556888 | ||||||
| chr11:58557090
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-2150A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557090 | ||||||
| chr11:58557289
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-2349C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557289 | ||||||
| chr11:58557404
|
T | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0159 | 3 | HG02602.hp1 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.219-2464A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557404 | ||||||
| chr11:58557412
|
G | C | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-2472C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557412 | ||||||
| chr11:58557545
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.219-2605T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557545 | ||||||
| chr11:58557600
|
T | C | 1 | a0001c0002t0001g0028 | 2 | NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.219-2660A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557600 | ||||||
| chr11:58557760
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219-2820A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557760 | ||||||
| chr11:58557773
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-2833G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557773 | ||||||
| chr11:58558018
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.219-3078G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558018 | ||||||
| chr11:58558031
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0063others(3): Show | 10 | NA18950.hp1 NA18951.hp2 NA18984.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-3091C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558031 | ||||||
| chr11:58558165
|
GA | G | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3226delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558165 | ||||||
| chr11:58558245
|
T | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.219-3305A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558245 | ||||||
| chr11:58558324
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.219-3384T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558324 | ||||||
| chr11:58558355
|
T | C | 2 | a0001c0002t0001g0036a0001c0002t0001g0204 | 3 | HG01099.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.219-3415A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558355 | ||||||
| chr11:58558405
|
C | T | 1 | a0001c0002t0001g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.219-3465G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558405 | ||||||
| chr11:58558417
|
G | A | 1 | a0003c0005t0001g0020 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219-3477C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558417 | ||||||
| chr11:58558540
|
C | CA | 22 | a0001c0001t0001g0019a0001c0001t0001g0075a0001c0001t0001g0099others(19): Show | 23 | HG00280.hp1 HG00609.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.219-3601dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | ||||||
| chr11:58558540
|
CA | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(83): Show | 123 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.219-3601delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | ||||||
| chr11:58558540
|
CAA | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0135others(8): Show | 13 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-3602_219-3601d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | ||||||
| chr11:58558796
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-3856A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558796 | ||||||
| chr11:58558801
|
A | G | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3861T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558801 | ||||||
| chr11:58558824
|
T | C | 4 | a0001c0002t0001g0032a0001c0002t0001g0185a0001c0002t0001g0186others(1): Show | 5 | HG01978.hp2 NA18950.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-3884A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558824 | ||||||
| chr11:58559157
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.219-4217T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559157 | ||||||
| chr11:58559245
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.219-4305A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559245 | ||||||
| chr11:58559322
|
G | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.219-4382C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559322 | ||||||
| chr11:58559374
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219-4434T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559374 | ||||||
| chr11:58559522
|
T | G | 4 | a0001c0002t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-4582A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559522 | ||||||
| chr11:58559704
|
C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(18): Show | 40 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.218+4451G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559704 | ||||||
| chr11:58559767
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+4388A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559767 | ||||||
| chr11:58559789
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.218+4366A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559789 | ||||||
| chr11:58559925
|
C | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218+4230G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559925 | ||||||
| chr11:58559954
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.218+4201G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559954 | ||||||
| chr11:58560231
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.218+3924T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560231 | ||||||
| chr11:58560492
|
T | C | 4 | a0001c0002t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+3663A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560492 | ||||||
| chr11:58560499
|
G | T | 2 | a0003c0005t0001g0111a0003c0005t0001g0112 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.218+3656C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560499 | ||||||
| chr11:58560997
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+3158T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560997 | ||||||
| chr11:58561106
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0196 | 6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+3049G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561106 | ||||||
| chr11:58561119
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.218+3036C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561119 | ||||||
| chr11:58561134
|
TTCTC | T | 7 | a0001c0001t0001g0041a0001c0002t0001g0146a0003c0005t0001g0020others(4): Show | 8 | HG00621.hp2 HG01496.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+3017_218+3020d others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561134 | ||||||
| chr11:58561256
|
G | A | 93 | a0001c0001t0001g0075a0001c0002t0001g0002a0001c0002t0001g0003others(90): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218+2899C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561256 | ||||||
| chr11:58561379
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+2776T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561379 | ||||||
| chr11:58561479
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.218+2676T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561479 | ||||||
| chr11:58561825
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218+2330A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561825 | ||||||
| chr11:58562496
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0231 | 7 | HG02280.hp2 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1659T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562496 | ||||||
| chr11:58562811
|
GT | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.218+1343delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562811 | ||||||
| chr11:58562813
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218+1342C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562813 | ||||||
| chr11:58562814
|
G | C | 3 | a0001c0002t0001g0160a0001c0002t0001g0188a0001c0002t0001g0209 | 3 | HG00280.hp2 HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.218+1341C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562814 | ||||||
| chr11:58562894
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.218+1261T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562894 | ||||||
| chr11:58563201
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218+954A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563201 | ||||||
| chr11:58563222
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+933A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563222 | ||||||
| chr11:58563836
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.218+319T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563836 | ||||||
| chr11:58563865
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+290G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563865 | ||||||
| chr11:58563917
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.218+238C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563917 | ||||||
| chr11:58563976
|
A | G | 1 | a0001c0001t0001g0023 | 2 | HG02071.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.218+179T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563976 | ||||||
| chr11:58564249
|
A | T | 1 | a0001c0002t0001g0030 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-48T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564249 | ||||||
| chr11:58564284
|
A | G | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-83T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564284 | ||||||
| chr11:58564367
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.172-166T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564367 | ||||||
| chr11:58564369
|
C | G | 3 | a0001c0002t0001g0160a0001c0002t0001g0188a0001c0002t0001g0209 | 3 | HG00280.hp2 HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.172-168G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564369 | ||||||
| chr11:58564395
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0100others(11): Show | 15 | HG00280.hp1 HG01884.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-194G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564395 | ||||||
| chr11:58564451
|
C | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 195 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.172-250G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564451 | ||||||
| chr11:58564930
|
G | A | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.172-729C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564930 | ||||||
| chr11:58564975
|
C | T | 1 | a0001c0002t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.172-774G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564975 | ||||||
| chr11:58564988
|
G | A | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-787C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564988 | ||||||
| chr11:58565073
|
G | A | 1 | a0001c0002t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.172-872C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565073 | ||||||
| chr11:58565138
|
T | A | 1 | a0001c0002t0001g0201 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172-937A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565138 | ||||||
| chr11:58565179
|
G | A | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-978C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565179 | ||||||
| chr11:58565260
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(16): Show | 25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.172-1059C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565260 | ||||||
| chr11:58565308
|
C | T | 1 | a0001c0002t0001g0158 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.172-1107G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565308 | ||||||
| chr11:58565329
|
C | G | 1 | a0001c0002t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-1128G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565329 | ||||||
| chr11:58565362
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.172-1161A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565362 | ||||||
| chr11:58565533
|
CA | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(69): Show | 96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.172-1333delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565533 | ||||||
| chr11:58565741
|
G | C | 1 | a0001c0001t0001g0039 | 2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.172-1540C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565741 | ||||||
| chr11:58565747
|
C | G | 1 | a0001c0002t0001g0157 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.172-1546G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565747 | ||||||
| chr11:58565891
|
G | C | 1 | a0001c0002t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.172-1690C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565891 | ||||||
| chr11:58565979
|
C | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0015others(34): Show | 47 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.172-1778G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565979 | ||||||
| chr11:58565985
|
G | T | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.172-1784C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565985 | ||||||
| chr11:58566132
|
CAT | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.172-1933_172-1932d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566132 | ||||||
| chr11:58566430
|
A | G | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-2229T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566430 | ||||||
| chr11:58566431
|
C | T | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-2230G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566431 | ||||||
| chr11:58566579
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(2): Show | 9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-2378A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566579 | ||||||
| chr11:58566615
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-2414T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566615 | ||||||
| chr11:58566620
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-2419A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566620 | ||||||
| chr11:58566630
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.172-2429T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566630 | ||||||
| chr11:58566670
|
G | A | 7 | a0001c0002t0001g0014a0001c0002t0001g0033a0001c0002t0001g0189others(4): Show | 10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-2469C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566670 | ||||||
| chr11:58566720
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.172-2519T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566720 | ||||||
| chr11:58566782
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-2581C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566782 | ||||||
| chr11:58566981
|
G | T | 1 | a0001c0002t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-2780C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566981 | ||||||
| chr11:58567000
|
C | CTG | 3 | a0001c0001t0001g0017a0001c0001t0001g0216a0001c0002t0001g0155 | 4 | HG00741.hp1 HG01167.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2801_172-2800d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567000 | ||||||
| chr11:58567000
|
CTG | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(34): Show | 46 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-2801_172-2800d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567000 | ||||||
| chr11:58567024
|
A | G | 1 | a0001c0002t0001g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172-2823T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567024 | ||||||
| chr11:58567095
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.172-2894C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567095 | ||||||
| chr11:58567174
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-2973T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567174 | ||||||
| chr11:58567197
|
G | T | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2996C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567197 | ||||||
| chr11:58567369
|
A | C | 1 | a0001c0002t0001g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.172-3168T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567369 | ||||||
| chr11:58567455
|
C | T | 9 | a0001c0002t0001g0013a0001c0002t0001g0027a0001c0002t0001g0028others(6): Show | 13 | HG00558.hp1 HG02015.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+3101G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567455 | ||||||
| chr11:58567665
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.171+2891G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567665 | ||||||
| chr11:58568070
|
A | G | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.171+2486T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568070 | ||||||
| chr11:58568075
|
A | G | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+2481T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568075 | ||||||
| chr11:58568077
|
C | T | 4 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148others(1): Show | 4 | HG00621.hp2 NA18942.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2479G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568077 | ||||||
| chr11:58568464
|
A | G | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171+2092T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568464 | ||||||
| chr11:58568506
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0050 | 2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.171+2050C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568506 | ||||||
| chr11:58568602
|
C | CA | 5 | a0001c0001t0001g0019a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 6 | HG00438.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1953dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568602 | ||||||
| chr11:58568602
|
CA | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(87): Show | 120 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.171+1953delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568602 | ||||||
| chr11:58568876
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(16): Show | 25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+1680T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568876 | ||||||
| chr11:58568943
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.171+1613C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568943 | ||||||
| chr11:58569071
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 195 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.171+1485C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569071 | ||||||
| chr11:58569147
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0122others(1): Show | 9 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1409C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569147 | ||||||
| chr11:58569378
|
T | G | 15 | a0001c0002t0001g0006a0001c0002t0001g0034a0001c0002t0001g0035others(12): Show | 22 | HG00642.hp2 HG00741.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.171+1178A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569378 | ||||||
| chr11:58569493
|
ATCC | A | 6 | a0001c0001t0001g0041a0003c0005t0001g0020a0003c0005t0001g0111others(3): Show | 7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1060_171+1062d others(5): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569493 | ||||||
| chr11:58569551
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.171+1005C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569551 | ||||||
| chr11:58569675
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0123 | 4 | HG00558.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+881G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569675 | ||||||
| chr11:58569816
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.171+740G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569816 | ||||||
| chr11:58569852
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0231 | 5 | HG02896.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+704C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569852 | ||||||
| chr11:58569944
|
A | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG00621.hp1 HG02523.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+612T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569944 | ||||||
| chr11:58570036
|
G | A | 1 | a0001c0002t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.171+520C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570036 | ||||||
| chr11:58570075
|
G | A | 3 | a0001c0002t0001g0036a0001c0002t0001g0203a0001c0002t0001g0204 | 4 | HG01099.hp1 HG02148.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+481C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570075 | ||||||
| chr11:58570082
|
T | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+474A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570082 | ||||||
| chr11:58570334
|
A | T | 1 | a0001c0002t0001g0025 | 2 | NA18965.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.171+222T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570334 | ||||||
| chr11:58570740
|
T | C | 1 | a0001c0002t0001g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.14-27A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570740 | ||||||
| chr11:58570820
|
A | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-107T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570820 | ||||||
| chr11:58570829
|
A | G | 1 | a0003c0005t0001g0020 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.14-116T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570829 | ||||||
| chr11:58571041
|
T | A | 1 | a0001c0002t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.14-328A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571041 | ||||||
| chr11:58571122
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.14-409G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571122 | ||||||
| chr11:58571155
|
T | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-442A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571155 | ||||||
| chr11:58571342
|
A | AAAAT | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(47): Show | 69 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.14-633_14-630dupAT others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | ||||||
| chr11:58571342
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 9 | HG01074.hp1 HG01255.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.14-637_14-630dupAT others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | ||||||
| chr11:58571342
|
AAAAT | A | 106 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0081others(103): Show | 149 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.14-633_14-630delAT others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | ||||||
| chr11:58571342
|
AAAATAAA others(1): Show |
A | 26 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0100others(23): Show | 29 | HG00280.hp1 HG01243.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.14-637_14-630delAT others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | ||||||
| chr11:58571562
|
T | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-849A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571562 | ||||||
| chr11:58571651
|
T | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-938A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571651 | ||||||
| chr11:58571663
|
C | CT | 13 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0100others(10): Show | 14 | HG00280.hp1 HG01884.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-951dupA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571663 | ||||||
| chr11:58571812
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.14-1099A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571812 | ||||||
| chr11:58571867
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14-1154C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571867 | ||||||
| chr11:58571943
|
T | C | 1 | a0001c0002t0001g0209 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.14-1230A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571943 | ||||||
| chr11:58572041
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.14-1328A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572041 | ||||||
| chr11:58572094
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.14-1381C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572094 | ||||||
| chr11:58572729
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.14-2016T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572729 | ||||||
| chr11:58573011
|
C | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-2298G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573011 | ||||||
| chr11:58573021
|
G | A | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14-2308C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573021 | ||||||
| chr11:58573072
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.14-2359G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573072 | ||||||
| chr11:58573186
|
C | T | 9 | a0002c0003t0001g0011a0002c0003t0001g0091a0002c0003t0001g0092others(6): Show | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-2473G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573186 | ||||||
| chr11:58573190
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.14-2477C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573190 | ||||||
| chr11:58573246
|
CAA | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.13+2512_13+2513del others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573246 | ||||||
| chr11:58573262
|
G | A | 1 | a0001c0002t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+2498C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573262 | ||||||
| chr11:58573263
|
A | G | 1 | a0001c0002t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+2497T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573263 | ||||||
| chr11:58573279
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.13+2481T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573279 | ||||||
| chr11:58573897
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+1863A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573897 | ||||||
| chr11:58573923
|
C | T | 1 | a0006c0008t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.13+1837G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573923 | ||||||
| chr11:58574033
|
CATTTCTC others(11): Show |
C | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.13+1709_13+1726del others(18): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574033 | ||||||
| chr11:58574547
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.13+1213G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574547 | ||||||
| chr11:58574608
|
G | A | 1 | a0001c0002t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+1152C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574608 | ||||||
| chr11:58574838
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.13+922G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574838 | ||||||
| chr11:58574877
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(18): Show | 40 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.13+883A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574877 | ||||||
| chr11:58575156
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0015others(34): Show | 47 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.13+604T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575156 | ||||||
| chr11:58575241
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13+519A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575241 | ||||||
| chr11:58575290
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0231 | 5 | HG02896.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+470G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575290 | ||||||
| chr11:58575336
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+424C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575336 | ||||||
| chr11:58575413
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.13+347G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575413 | ||||||
| chr11:58575425
|
A | C | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.13+335T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575425 | ||||||
| chr11:58575748
|
C | G | 2 | a0001c0001t0001g0041a0006c0008t0001g0040 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.13+12G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575748 |