Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4046 |
| ensemblid | ENSG00000130592.17 |
| hgncid | 6707 |
| symbol | LSP1 |
| name | lymphocyte specific protein 1 |
| refseq_nuc | NM_002339.3 |
| refseq_prot | NP_002330.1 |
| ensembl_nuc | ENST00000311604.8 |
| ensembl_prot | ENSP00000308383.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 1853084 |
| end | 1892263 |
| strand | + |
| ver | v1.2 |
| region | chr11:1853084-1892263 |
| region5000 | chr11:1848084-1897263 |
| regionname0 | LSP1_chr11_1853084_1892263 |
| regionname5000 | LSP1_chr11_1848084_1897263 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 339 | 147 | 18 | 39 | 68 | 8 | 14 | 45 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002 | 1/1 | 339 | 143 | 36 | 27 | 50 | 7 | 21 | 37 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0003 | 0/0 | 339 | 63 | 24 | 12 | 23 | 1 | 3 | 12 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0004 | 0/0 | 339 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0005 | 0/0 | 339 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0006 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0007 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0008 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1020 | 111 | 24 | 23 | 39 | 7 | 16 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0002 | 0/0 | 1020 | 74 | 3 | 20 | 44 | 3 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0003 | 0/0 | 1020 | 72 | 15 | 19 | 23 | 5 | 10 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0004 | 0/0 | 1020 | 47 | 16 | 10 | 18 | 0 | 3 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0005 | 0/0 | 1020 | 25 | 9 | 2 | 10 | 0 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0006 | 0/0 | 1020 | 16 | 8 | 2 | 5 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0007 | 0/0 | 1020 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0008 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0009 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0010 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0011 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0012 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0013 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0014 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0015 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0016 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0017 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| c0018 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 566 | 335 | 73 | 69 | 140 | 15 | 37 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0002 | 1/0 | 566 | 12 | 3 | 7 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0003 | 0/0 | 566 | 4 | 4 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0004 | 0/0 | 566 | 3 | 2 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0005 | 0/0 | 566 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0006 | 0/0 | 566 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0007 | 0/0 | 566 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0008 | 0/0 | 566 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0009 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| t0010 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0002 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0003 | 0/0 | 7 | 0 | 3 | 0 | 3 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0009 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1020 | 74 | 3 | 20 | 44 | 3 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0001c0003 | 0/0 | 1020 | 72 | 15 | 19 | 23 | 5 | 10 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0001c0018 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0001 | 1/1 | 1020 | 111 | 24 | 23 | 39 | 7 | 16 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0005 | 0/0 | 1020 | 25 | 9 | 2 | 10 | 0 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0007 | 0/0 | 1020 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0011 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0012 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0013 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0016 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0002c0017 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0003c0004 | 0/0 | 1020 | 47 | 16 | 10 | 18 | 0 | 3 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0003c0006 | 0/0 | 1020 | 16 | 8 | 2 | 5 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0004c0008 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0005c0009 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0006c0014 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0007c0015 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 | |
| a0008c0010 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 1585 | 74 | 3 | 20 | 44 | 3 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0001c0003t0001 | 0/0 | 1585 | 71 | 15 | 18 | 23 | 5 | 10 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0001c0003t0008 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0001c0018t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0001 | 0/1 | 1585 | 94 | 19 | 16 | 37 | 6 | 15 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0002 | 1/0 | 1585 | 11 | 3 | 6 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0004 | 0/0 | 1585 | 3 | 2 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0005 | 0/0 | 1585 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0006 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0001t0007 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0005t0001 | 0/0 | 1585 | 23 | 7 | 2 | 10 | 0 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0005t0003 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0005t0009 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0007t0001 | 0/0 | 1585 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0011t0010 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0012t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0013t0001 | 0/0 | 1585 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0016t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0002c0017t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0003c0004t0001 | 0/0 | 1585 | 44 | 14 | 9 | 18 | 0 | 3 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0003c0004t0002 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0003c0004t0003 | 0/0 | 1585 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0003c0006t0001 | 0/0 | 1585 | 16 | 8 | 2 | 5 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0004c0008t0001 | 0/0 | 1585 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0005c0009t0001 | 0/0 | 1585 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0006c0014t0003 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0007c0015t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| a0008c0010t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | copy fasta | chr11 | 1848084 | 1897263 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 3 | 0 | 3 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0001 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0003t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0001c0018t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0009 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0002g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0005t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0007t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0007t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0011t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0012t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0013t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0016t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0002c0017t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0003c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0004c0008t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0004c0008t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0005c0009t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0005c0009t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0006c0014t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0007c0015t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| a0008c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0072 | EUR | GBR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0078 | EUR | GBR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0081 | EUR | FIN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00280 | hp2 | a0002 | c0001 | t0002 | g0177 | EUR | FIN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0267 | EUR | FIN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0215 | EUR | FIN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0240 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0256 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0076 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0080 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00558 | hp2 | a0002 | c0005 | t0001 | g0097 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00597 | hp2 | a0003 | c0004 | t0001 | g0211 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00609 | hp2 | a0003 | c0006 | t0001 | g0102 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0278 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00639 | hp1 | a0002 | c0005 | t0001 | g0027 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0241 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00642 | hp2 | a0003 | c0006 | t0001 | g0028 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00673 | hp1 | a0002 | c0005 | t0001 | g0134 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | CHS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0282 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00733 | hp2 | a0003 | c0004 | t0001 | g0178 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00735 | hp1 | a0002 | c0001 | t0002 | g0041 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00735 | hp2 | a0002 | c0007 | t0001 | g0261 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0231 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG00741 | hp2 | a0003 | c0004 | t0001 | g0222 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01070 | hp1 | a0002 | c0001 | t0002 | g0016 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01070 | hp2 | a0003 | c0004 | t0001 | g0032 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01071 | hp1 | a0002 | c0001 | t0002 | g0020 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0016 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01074 | hp2 | a0002 | c0005 | t0001 | g0147 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0232 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01099 | hp2 | a0002 | c0001 | t0002 | g0020 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0262 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0223 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01109 | hp1 | a0003 | c0004 | t0002 | g0219 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01109 | hp2 | a0002 | c0007 | t0001 | g0260 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0281 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0035 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0035 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01192 | hp2 | a0002 | c0001 | t0002 | g0016 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0244 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01243 | hp2 | a0002 | c0001 | t0004 | g0190 | AMR | PUR | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0201 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0159 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0230 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01346 | hp2 | a0003 | c0006 | t0001 | g0149 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0263 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0083 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0162 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0001 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0017 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0203 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | IBS | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01884 | hp2 | a0002 | c0005 | t0001 | g0086 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0257 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0044 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0197 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0207 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02027 | hp2 | a0003 | c0006 | t0001 | g0013 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0214 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02129 | hp2 | a0002 | c0005 | t0001 | g0013 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0202 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02135 | hp1 | a0002 | c0005 | t0001 | g0013 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02145 | hp1 | a0003 | c0004 | t0001 | g0210 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02145 | hp2 | a0003 | c0004 | t0001 | g0036 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0238 | EAS | CDX | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02155 | hp2 | a0008 | c0010 | t0001 | g0064 | EAS | CDX | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0236 | EAS | CDX | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02165 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | CDX | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0189 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02258 | hp2 | a0002 | c0001 | t0004 | g0030 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0161 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02280 | hp2 | a0005 | c0009 | t0001 | g0171 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0036 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02451 | hp2 | a0003 | c0004 | t0003 | g0196 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02523 | hp1 | a0003 | c0006 | t0001 | g0103 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02523 | hp2 | a0002 | c0005 | t0001 | g0119 | EAS | KHV | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0191 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02602 | hp1 | a0002 | c0005 | t0001 | g0090 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0274 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02615 | hp1 | a0003 | c0004 | t0001 | g0208 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02615 | hp2 | a0002 | c0001 | t0001 | g0194 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0209 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02622 | hp2 | a0003 | c0006 | t0001 | g0154 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02630 | hp1 | a0005 | c0009 | t0001 | g0172 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02630 | hp2 | a0003 | c0006 | t0001 | g0156 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02647 | hp1 | a0002 | c0005 | t0001 | g0099 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0247 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0009 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02698 | hp1 | a0002 | c0005 | t0001 | g0158 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0270 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0170 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02723 | hp1 | a0002 | c0001 | t0002 | g0180 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02723 | hp2 | a0003 | c0006 | t0001 | g0028 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02735 | hp2 | a0002 | c0001 | t0005 | g0266 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0242 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02818 | hp2 | a0002 | c0005 | t0001 | g0151 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02886 | hp2 | a0003 | c0004 | t0003 | g0187 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0218 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02896 | hp2 | a0002 | c0001 | t0001 | g0188 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02922 | hp1 | a0003 | c0006 | t0001 | g0087 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02965 | hp1 | a0002 | c0001 | t0004 | g0030 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0193 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02970 | hp1 | a0002 | c0016 | t0001 | g0098 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02976 | hp2 | a0002 | c0001 | t0002 | g0175 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0280 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0067 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0186 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03041 | hp2 | a0002 | c0017 | t0001 | g0153 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0220 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03130 | hp2 | a0006 | c0014 | t0003 | g0199 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0182 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0250 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03195 | hp2 | a0002 | c0001 | t0001 | g0163 | AFR | ESN | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0225 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0027 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0084 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03453 | hp1 | a0007 | c0015 | t0001 | g0145 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0192 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03486 | hp1 | a0004 | c0008 | t0001 | g0164 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03486 | hp2 | a0002 | c0005 | t0009 | g0085 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0021 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0071 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0021 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0216 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0195 | AFR | GWD | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0015 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0032 | AFR | MSL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0045 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03669 | hp2 | a0002 | c0005 | t0001 | g0093 | SAS | PJL | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0010 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0235 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03834 | hp2 | a0002 | c0013 | t0001 | g0068 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0063 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03927 | hp2 | a0003 | c0004 | t0001 | g0224 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0248 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0279 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0165 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | BEB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0275 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04204 | hp2 | a0003 | c0004 | t0001 | g0286 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04228 | hp1 | a0003 | c0004 | t0001 | g0227 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0264 | SAS | STU | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18522 | hp2 | a0003 | c0006 | t0001 | g0015 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0226 | EAS | CHB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18612 | hp2 | a0003 | c0004 | t0001 | g0060 | EAS | CHB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | CHB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18906 | hp2 | a0003 | c0004 | t0001 | g0213 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18942 | hp1 | a0003 | c0004 | t0001 | g0239 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0269 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18943 | hp2 | a0002 | c0005 | t0001 | g0130 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18948 | hp2 | a0002 | c0005 | t0001 | g0142 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18950 | hp1 | a0003 | c0004 | t0001 | g0283 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0233 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18952 | hp1 | a0002 | c0012 | t0001 | g0006 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0276 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18969 | hp2 | a0002 | c0005 | t0001 | g0133 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0284 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0273 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0268 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18980 | hp2 | a0003 | c0006 | t0001 | g0157 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18993 | hp1 | a0002 | c0001 | t0007 | g0006 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18997 | hp1 | a0002 | c0005 | t0001 | g0118 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18997 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0272 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18998 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18999 | hp1 | a0002 | c0001 | t0006 | g0245 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0217 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19004 | hp2 | a0003 | c0004 | t0001 | g0212 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | LWK | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0254 | AFR | LWK | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19057 | hp1 | a0002 | c0005 | t0001 | g0126 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19066 | hp1 | a0003 | c0006 | t0001 | g0120 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0228 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19067 | hp2 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0204 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19077 | hp1 | a0001 | c0018 | t0001 | g0137 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19081 | hp2 | a0003 | c0004 | t0001 | g0237 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0271 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0277 | EAS | JPT | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19240 | hp1 | a0003 | c0006 | t0001 | g0152 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | YRI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20129 | hp1 | a0003 | c0004 | t0001 | g0221 | AFR | ASW | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0253 | AFR | ASW | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20752 | hp2 | a0003 | c0006 | t0001 | g0234 | EUR | TSI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0055 | EUR | TSI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0077 | EUR | TSI | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0166 | SAS | GIH | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20905 | hp2 | a0002 | c0005 | t0001 | g0092 | SAS | GIH | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0082 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG01123 | hp2 | a0001 | c0003 | t0008 | g0051 | AMR | CLM | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02486 | hp1 | a0003 | c0006 | t0001 | g0015 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02486 | hp2 | a0002 | c0005 | t0001 | g0148 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02559 | hp1 | a0002 | c0001 | t0002 | g0176 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG02559 | hp2 | a0004 | c0008 | t0001 | g0183 | AFR | ACB | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG06807 | hp1 | a0002 | c0005 | t0003 | g0155 | AFR | USA | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | USA | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0169 | AFR | USA | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA20300 | hp2 | a0003 | c0006 | t0001 | g0150 | AFR | USA | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0091 | AFR | LWK | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| NA21309 | hp2 | a0002 | c0011 | t0010 | g0173 | AFR | LWK | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0009 | REF | REF | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0002 | g0243 | REF | REF | LSP1_chr11_1848084_1897263 | LSP1 | chr11 | 1848084 | 1897263 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1880205 | C | T | 1 | a0005 | 2 | HG02280.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.172C>T | p.Arg58Trp | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/11 | 233/1585 | 172/1020 | 58/339 | chr11 | 1880205 | ||
| chr11:1881538 | G | A | 4 | a0001a0005a0007others(1): Show | 151 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
missense_variant | MODERATE | c.298G>A | p.Ala100Thr | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/11 | 359/1585 | 298/1020 | 100/339 | chr11 | 1881538 | ||
| chr11:1881551 | G | C | 1 | a0004 | 2 | HG02559.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.311G>C | p.Gly104Ala | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/11 | 372/1585 | 311/1020 | 104/339 | chr11 | 1881551 | ||
| chr11:1881563 | A | T | 2 | a0003a0006 | 64 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.323A>T | p.Gln108Leu | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/11 | 384/1585 | 323/1020 | 108/339 | chr11 | 1881563 | ||
| chr11:1884286 | G | T | 1 | a0008 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.598G>T | p.Asp200Tyr | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 6/11 | 659/1585 | 598/1020 | 200/339 | chr11 | 1884286 | ||
| chr11:1886777 | C | A | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.763C>A | p.Leu255Met | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 8/11 | 824/1585 | 763/1020 | 255/339 | chr11 | 1886777 | ||
| chr11:1886840 | T | G | 1 | a0006 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.826T>G | p.Ser276Ala | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 8/11 | 887/1585 | 826/1020 | 276/339 | chr11 | 1886840 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1853174 | C | T | 7 | a0001c0002a0001c0018a0002c0005others(4): Show | 119 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(116): Show |
synonymous_variant | LOW | c.30C>T | p.Ala10Ala | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/11 | 91/1585 | 30/1020 | 10/339 | chr11 | 1853174 | ||
| chr11:1880132 | C | T | 1 | a0001c0018 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.99C>T | p.His33His | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/11 | 160/1585 | 99/1020 | 33/339 | chr11 | 1880132 | ||
| chr11:1881522 | C | T | 1 | a0002c0017 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.282C>T | p.His94His | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/11 | 343/1585 | 282/1020 | 94/339 | chr11 | 1881522 | ||
| chr11:1881541 | T | C | 1 | a0002c0007 | 2 | HG00735.hp2 HG01109.hp2 |
synonymous_variant | LOW | c.301T>C | p.Leu101Leu | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/11 | 362/1585 | 301/1020 | 101/339 | chr11 | 1881541 | ||
| chr11:1883988 | C | T | 1 | a0002c0013 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.555C>T | p.Ile185Ile | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 5/11 | 616/1585 | 555/1020 | 185/339 | chr11 | 1883988 | ||
| chr11:1884518 | C | A | 1 | a0002c0011 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.654C>A | p.Ser218Ser | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/11 | 715/1585 | 654/1020 | 218/339 | chr11 | 1884518 | ||
| chr11:1884569 | C | T | 1 | a0002c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.705C>T | p.Thr235Thr | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/11 | 766/1585 | 705/1020 | 235/339 | chr11 | 1884569 | ||
| chr11:1887551 | C | A | 1 | a0002c0012 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1008C>A | p.Gly336Gly | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/11 | 1069/1585 | 1008/1020 | 336/339 | chr11 | 1887551 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1891843 | G | C | 1 | a0002c0001t0005 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4280 | chr11 | 1891843 | |||||
| chr11:1891914 | C | T | 1 | a0002c0011t0010 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4351 | chr11 | 1891914 | |||||
| chr11:1891976 | C | T | 2 | a0002c0001t0004a0002c0005t0009 | 4 | HG01243.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4413 | chr11 | 1891976 | |||||
| chr11:1892038 | T | G | 1 | a0002c0001t0006 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4475 | chr11 | 1892038 | |||||
| chr11:1892099 | G | A | 1 | a0002c0001t0007 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4536 | chr11 | 1892099 | |||||
| chr11:1892147 | A | G | 26 | a0001c0002t0001a0001c0003t0001a0001c0003t0008others(23): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*388A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4584 | chr11 | 1892147 | |||||
| chr11:1892178 | A | G | 3 | a0002c0005t0003a0003c0004t0003a0006c0014t0003 | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*419A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4615 | chr11 | 1892178 | |||||
| chr11:1892206 | G | A | 2 | a0001c0003t0008a0002c0005t0009 | 2 | HG01123.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 11/11 | 4643 | chr11 | 1892206 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1853216 | G | A | 5 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(2): Show | 8 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+19G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853216 | ||||||
| chr11:1853311 | A | G | 1 | a0001c0003t0001g0287 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53+114A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853311 | ||||||
| chr11:1853415 | G | A | 1 | a0002c0001t0002g0041 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.53+218G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853415 | ||||||
| chr11:1853615 | T | C | 195 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(192): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.53+418T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853615 | ||||||
| chr11:1853662 | G | A | 39 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(36): Show | 54 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.53+465G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853662 | ||||||
| chr11:1853706 | A | G | 1 | a0003c0004t0001g0036 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.53+509A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853706 | ||||||
| chr11:1853713 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+516C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853713 | ||||||
| chr11:1853734 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+537G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853734 | ||||||
| chr11:1853774 | T | C | 1 | a0002c0001t0001g0075 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.53+577T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853774 | ||||||
| chr11:1853837 | G | A | 53 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(50): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.53+640G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853837 | ||||||
| chr11:1853848 | A | G | 1 | a0001c0003t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.53+651A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853848 | ||||||
| chr11:1853858 | A | G | 15 | a0001c0003t0001g0198a0002c0001t0001g0008a0002c0001t0001g0188others(12): Show | 19 | HG01243.hp2 HG01943.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.53+661A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853858 | ||||||
| chr11:1853869 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+672G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853869 | ||||||
| chr11:1853894 | G | C | 137 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(134): Show | 174 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.53+697G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853894 | ||||||
| chr11:1853994 | G | A | 4 | a0001c0002t0001g0200a0002c0005t0001g0086a0002c0005t0009g0085others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+797G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1853994 | ||||||
| chr11:1854004 | C | T | 1 | a0001c0002t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.53+807C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854004 | ||||||
| chr11:1854028 | C | T | 1 | a0006c0014t0003g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53+831C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854028 | ||||||
| chr11:1854052 | C | T | 4 | a0001c0002t0001g0200a0001c0003t0001g0184a0001c0003t0001g0185others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+855C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854052 | ||||||
| chr11:1854059 | G | T | 44 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(41): Show | 52 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.53+862G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854059 | ||||||
| chr11:1854092 | C | T | 1 | a0002c0005t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.53+895C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854092 | ||||||
| chr11:1854133 | C | T | 8 | a0001c0003t0001g0179a0002c0001t0002g0016a0002c0001t0002g0041others(5): Show | 10 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+936C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854133 | ||||||
| chr11:1854157 | A | T | 1 | a0001c0003t0001g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53+960A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854157 | ||||||
| chr11:1854179 | C | T | 2 | a0003c0004t0001g0286a0003c0006t0001g0157 | 2 | HG04204.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.53+982C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854179 | ||||||
| chr11:1854199 | G | A | 1 | a0002c0001t0001g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.53+1002G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854199 | ||||||
| chr11:1854270 | G | A | 2 | a0001c0003t0001g0184a0001c0003t0001g0185 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.53+1073G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854270 | ||||||
| chr11:1854281 | C | T | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(84): Show | 113 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.53+1084C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854281 | ||||||
| chr11:1854378 | C | T | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+1181C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854378 | ||||||
| chr11:1854552 | C | A | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1355C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854552 | ||||||
| chr11:1854553 | A | C | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1356A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854553 | ||||||
| chr11:1854554 | C | A | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1357C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854554 | ||||||
| chr11:1854581 | A | G | 3 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.53+1384A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854581 | ||||||
| chr11:1854624 | G | T | 1 | a0003c0006t0001g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53+1427G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854624 | ||||||
| chr11:1854653 | C | T | 1 | a0004c0008t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+1456C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854653 | ||||||
| chr11:1854656 | C | T | 2 | a0001c0003t0001g0072a0001c0003t0001g0073 | 2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.53+1459C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854656 | ||||||
| chr11:1854756 | C | T | 1 | a0002c0005t0003g0155 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.53+1559C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854756 | ||||||
| chr11:1854761 | C | T | 94 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(91): Show | 122 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.53+1564C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854761 | ||||||
| chr11:1854774 | C | G | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1577C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854774 | ||||||
| chr11:1854782 | A | C | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1585A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854782 | ||||||
| chr11:1854783 | G | A | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1586G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854783 | ||||||
| chr11:1854784 | C | G | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.53+1587C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854784 | ||||||
| chr11:1854796 | T | G | 1 | a0002c0001t0001g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.53+1599T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854796 | ||||||
| chr11:1854866 | T | A | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.53+1669T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854866 | ||||||
| chr11:1854927 | G | A | 54 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(51): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.53+1730G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854927 | ||||||
| chr11:1854956 | C | T | 121 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(118): Show | 153 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.53+1759C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854956 | ||||||
| chr11:1854981 | C | T | 1 | a0002c0005t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53+1784C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854981 | ||||||
| chr11:1854998 | C | T | 76 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(73): Show | 101 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.53+1801C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1854998 | ||||||
| chr11:1855030 | C | T | 8 | a0001c0003t0001g0179a0002c0001t0002g0016a0002c0001t0002g0041others(5): Show | 10 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+1833C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855030 | ||||||
| chr11:1855059 | C | T | 1 | a0002c0001t0001g0197 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.53+1862C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855059 | ||||||
| chr11:1855091 | C | A | 1 | a0002c0001t0001g0197 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.53+1894C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855091 | ||||||
| chr11:1855171 | G | T | 17 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186others(14): Show | 21 | HG01243.hp2 HG01943.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.53+1974G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855171 | ||||||
| chr11:1855324 | A | G | 121 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(118): Show | 153 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.53+2127A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855324 | ||||||
| chr11:1855364 | C | T | 22 | a0001c0003t0001g0270a0002c0001t0001g0009a0002c0001t0001g0201others(19): Show | 25 | HG00323.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.53+2167C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855364 | ||||||
| chr11:1855365 | G | A | 120 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(117): Show | 152 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.53+2168G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855365 | ||||||
| chr11:1855445 | A | C | 1 | a0002c0001t0001g0284 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.53+2248A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855445 | ||||||
| chr11:1855487 | C | T | 122 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(119): Show | 154 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.53+2290C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855487 | ||||||
| chr11:1855544 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.53+2347C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855544 | ||||||
| chr11:1855637 | C | T | 55 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(52): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.53+2440C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855637 | ||||||
| chr11:1855656 | C | T | 3 | a0003c0006t0001g0028a0003c0006t0001g0154a0003c0006t0001g0156 | 4 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+2459C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855656 | ||||||
| chr11:1855715 | G | A | 55 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(52): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.53+2518G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855715 | ||||||
| chr11:1855725 | A | C | 194 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(191): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.53+2528A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855725 | ||||||
| chr11:1855841 | C | T | 122 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(119): Show | 154 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.53+2644C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855841 | ||||||
| chr11:1855969 | A | G | 1 | a0003c0004t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.53+2772A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1855969 | ||||||
| chr11:1856044 | C | T | 55 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(52): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.53+2847C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856044 | ||||||
| chr11:1856078 | C | T | 1 | a0001c0003t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.53+2881C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856078 | ||||||
| chr11:1856079 | G | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG01099.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.53+2882G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856079 | ||||||
| chr11:1856126 | T | C | 1 | a0001c0003t0001g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.53+2929T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856126 | ||||||
| chr11:1856135 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.53+2938C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856135 | ||||||
| chr11:1856208 | A | G | 121 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(118): Show | 153 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.53+3011A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856208 | ||||||
| chr11:1856209 | C | G | 1 | a0001c0002t0001g0096 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.53+3012C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856209 | ||||||
| chr11:1856252 | G | C | 1 | a0002c0001t0005g0266 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53+3055G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856252 | ||||||
| chr11:1856282 | C | G | 123 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(120): Show | 155 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.53+3085C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856282 | ||||||
| chr11:1856289 | C | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(65): Show | 91 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.53+3092C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856289 | ||||||
| chr11:1856303 | T | C | 196 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(193): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.53+3106T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856303 | ||||||
| chr11:1856462 | G | A | 2 | a0002c0001t0002g0175a0002c0001t0002g0176 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.53+3265G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856462 | ||||||
| chr11:1856600 | G | A | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+3403G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856600 | ||||||
| chr11:1856617 | T | C | 124 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(121): Show | 157 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.53+3420T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856617 | ||||||
| chr11:1856843 | G | A | 122 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(119): Show | 154 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.53+3646G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856843 | ||||||
| chr11:1856863 | C | T | 1 | a0007c0015t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.53+3666C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1856863 | ||||||
| chr11:1857029 | A | G | 1 | a0002c0001t0001g0159 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.53+3832A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857029 | ||||||
| chr11:1857176 | C | T | 48 | a0001c0003t0001g0258a0001c0003t0001g0265a0001c0003t0001g0270others(45): Show | 54 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.53+3979C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857176 | ||||||
| chr11:1857191 | C | T | 14 | a0002c0001t0001g0008a0002c0001t0001g0188a0002c0001t0001g0189others(11): Show | 18 | HG01243.hp2 HG01943.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.53+3994C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857191 | ||||||
| chr11:1857232 | T | C | 123 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(120): Show | 156 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.53+4035T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857232 | ||||||
| chr11:1857296 | C | A | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.53+4099C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857296 | ||||||
| chr11:1857344 | A | G | 123 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(120): Show | 156 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.53+4147A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857344 | ||||||
| chr11:1857357 | G | A | 1 | a0002c0001t0001g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.53+4160G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857357 | ||||||
| chr11:1857406 | A | G | 123 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(120): Show | 156 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.53+4209A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857406 | ||||||
| chr11:1857539 | C | A | 1 | a0002c0001t0001g0244 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.53+4342C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857539 | ||||||
| chr11:1857591 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+4394G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857591 | ||||||
| chr11:1857664 | C | T | 1 | a0001c0003t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.53+4467C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857664 | ||||||
| chr11:1857727 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+4530C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857727 | ||||||
| chr11:1857871 | C | G | 67 | a0001c0002t0001g0144a0001c0003t0001g0001a0001c0003t0001g0004others(64): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.53+4674C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1857871 | ||||||
| chr11:1858046 | G | A | 2 | a0001c0003t0001g0168a0002c0005t0009g0085 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.53+4849G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858046 | ||||||
| chr11:1858096 | C | T | 55 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0010others(52): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.53+4899C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858096 | ||||||
| chr11:1858138 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53+4941C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858138 | ||||||
| chr11:1858169 | T | C | 2 | a0002c0001t0001g0077a0002c0001t0001g0078 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.53+4972T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858169 | ||||||
| chr11:1858295 | T | C | 1 | a0002c0005t0001g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.53+5098T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858295 | ||||||
| chr11:1858393 | G | A | 1 | a0001c0003t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53+5196G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858393 | ||||||
| chr11:1858404 | G | A | 1 | a0001c0003t0001g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.53+5207G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858404 | ||||||
| chr11:1858412 | G | A | 1 | a0002c0001t0001g0079 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.53+5215G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858412 | ||||||
| chr11:1858422 | C | T | 1 | a0007c0015t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.53+5225C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858422 | ||||||
| chr11:1858423 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.53+5226G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858423 | ||||||
| chr11:1858558 | A | G | 3 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.53+5361A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858558 | ||||||
| chr11:1858714 | C | T | 85 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(82): Show | 114 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.53+5517C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858714 | ||||||
| chr11:1858760 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.53+5563G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858760 | ||||||
| chr11:1858963 | C | T | 2 | a0002c0005t0001g0092a0002c0005t0001g0093 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.53+5766C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1858963 | ||||||
| chr11:1859047 | G | C | 1 | a0003c0004t0001g0204 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.53+5850G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859047 | ||||||
| chr11:1859084 | T | A | 288 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(285): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.53+5887T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859084 | ||||||
| chr11:1859188 | G | A | 12 | a0001c0003t0001g0285a0002c0001t0001g0029a0002c0001t0001g0075others(9): Show | 13 | HG01433.hp2 HG02132.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+5991G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859188 | ||||||
| chr11:1859246 | T | C | 180 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(177): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.53+6049T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859246 | ||||||
| chr11:1859366 | C | G | 68 | a0001c0002t0001g0144a0001c0003t0001g0001a0001c0003t0001g0004others(65): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.53+6169C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859366 | ||||||
| chr11:1859378 | G | A | 11 | a0001c0003t0001g0285a0002c0001t0001g0029a0002c0001t0001g0075others(8): Show | 12 | HG01433.hp2 HG02132.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+6181G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859378 | ||||||
| chr11:1859451 | T | G | 1 | a0001c0003t0001g0285 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.53+6254T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859451 | ||||||
| chr11:1859500 | C | A | 7 | a0001c0003t0001g0179a0002c0001t0002g0016a0002c0001t0002g0041others(4): Show | 9 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+6303C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859500 | ||||||
| chr11:1859534 | C | A | 1 | a0002c0001t0001g0267 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.53+6337C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859534 | ||||||
| chr11:1859552 | G | A | 36 | a0001c0002t0001g0022a0001c0003t0001g0258a0001c0003t0001g0265others(33): Show | 44 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.53+6355G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859552 | ||||||
| chr11:1859574 | C | G | 1 | a0003c0006t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+6377C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859574 | ||||||
| chr11:1859581 | G | A | 179 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(176): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+6384G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859581 | ||||||
| chr11:1859593 | T | A | 1 | a0001c0002t0001g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.53+6396T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859593 | ||||||
| chr11:1859606 | C | A | 1 | a0001c0003t0001g0046 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.53+6409C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859606 | ||||||
| chr11:1859690 | TCCAGCCC others(7): Show |
T | 1 | a0002c0001t0001g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.53+6513_53+6526del others(14): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1859690 | |||||
| chr11:1859709 | C | T | 1 | a0001c0003t0001g0069 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.53+6512C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859709 | ||||||
| chr11:1859726 | C | T | 2 | a0001c0003t0001g0179a0003c0004t0001g0178 | 2 | HG00639.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.53+6529C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859726 | ||||||
| chr11:1859806 | C | T | 11 | a0001c0003t0001g0011a0001c0003t0001g0045a0001c0003t0001g0061others(8): Show | 13 | HG00673.hp2 HG02080.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.53+6609C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859806 | ||||||
| chr11:1859823 | T | C | 1 | a0002c0001t0001g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53+6626T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859823 | ||||||
| chr11:1859841 | G | A | 179 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(176): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+6644G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1859841 | ||||||
| chr11:1860021 | C | T | 6 | a0002c0001t0001g0264a0002c0005t0001g0090a0002c0005t0001g0091others(3): Show | 6 | HG02602.hp1 HG02698.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+6824C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860021 | ||||||
| chr11:1860026 | T | C | 216 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(213): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.53+6829T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860026 | ||||||
| chr11:1860044 | C | G | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53+6847C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860044 | ||||||
| chr11:1860132 | C | T | 1 | a0002c0005t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.53+6935C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860132 | ||||||
| chr11:1860290 | T | C | 6 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(3): Show | 9 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+7093T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860290 | ||||||
| chr11:1860294 | A | G | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.53+7097A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860294 | ||||||
| chr11:1860295 | T | TGATGGAT others(1): Show |
37 | a0001c0002t0001g0022a0001c0003t0001g0258a0001c0003t0001g0265others(34): Show | 45 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.53+7104_53+7111dup others(8): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1860295 | |||||
| chr11:1860295 | T | TGATGGAT others(5): Show |
179 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(176): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+7100_53+7111dup others(12): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1860295 | |||||
| chr11:1860381 | A | T | 1 | a0001c0002t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53+7184A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860381 | ||||||
| chr11:1860398 | A | G | 8 | a0001c0003t0001g0179a0002c0001t0002g0016a0002c0001t0002g0041others(5): Show | 10 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+7201A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860398 | ||||||
| chr11:1860748 | C | T | 37 | a0001c0002t0001g0022a0001c0003t0001g0258a0001c0003t0001g0265others(34): Show | 45 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.53+7551C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860748 | ||||||
| chr11:1860810 | T | C | 1 | a0003c0004t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.53+7613T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860810 | ||||||
| chr11:1860825 | A | T | 1 | a0001c0002t0001g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53+7628A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1860825 | ||||||
| chr11:1860849 | T | TATGGGTG others(9): Show |
189 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(186): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.53+7664_53+7665ins others(16): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1860849 | |||||
| chr11:1861018 | T | C | 181 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(178): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.53+7821T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861018 | ||||||
| chr11:1861019 | C | G | 1 | a0002c0005t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53+7822C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861019 | ||||||
| chr11:1861232 | C | G | 1 | a0002c0001t0002g0041 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.53+8035C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861232 | ||||||
| chr11:1861233 | G | A | 6 | a0001c0003t0001g0168a0001c0003t0001g0170a0001c0003t0001g0174others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+8036G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861233 | ||||||
| chr11:1861240 | A | G | 2 | a0005c0009t0001g0171a0005c0009t0001g0172 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.53+8043A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861240 | ||||||
| chr11:1861610 | G | T | 1 | a0003c0004t0001g0283 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.53+8413G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861610 | ||||||
| chr11:1861681 | G | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+8484G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861681 | ||||||
| chr11:1861687 | A | G | 1 | a0003c0004t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.53+8490A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861687 | ||||||
| chr11:1861695 | G | A | 1 | a0003c0004t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.53+8498G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861695 | ||||||
| chr11:1861695 | G | GTGGA | 15 | a0002c0001t0001g0207a0002c0001t0001g0214a0002c0001t0001g0268others(12): Show | 16 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+8540_53+8543dup others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1861695 | |||||
| chr11:1861695 | GTGGA | G | 185 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(182): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.53+8540_53+8543del others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1861695 | |||||
| chr11:1861695 | GTGGATGG others(1): Show |
G | 3 | a0001c0002t0001g0143a0002c0001t0002g0177a0005c0009t0001g0172 | 3 | HG00280.hp2 HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.53+8536_53+8543del others(8): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1861695 | |||||
| chr11:1861699 | A | G | 1 | a0002c0001t0001g0259 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.53+8502A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861699 | ||||||
| chr11:1861703 | A | G | 6 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(3): Show | 9 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+8506A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861703 | ||||||
| chr11:1861792 | T | C | 1 | a0002c0001t0001g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.53+8595T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861792 | ||||||
| chr11:1861904 | CGGAT | C | 190 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(187): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.53+8732_53+8735del others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1861904 | |||||
| chr11:1861944 | T | A | 35 | a0001c0003t0001g0179a0001c0003t0001g0184a0001c0003t0001g0185others(32): Show | 42 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.53+8747T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1861944 | ||||||
| chr11:1861978 | GATGGATG others(5): Show |
G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+8793_53+8804del others(12): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1861978 | |||||
| chr11:1862196 | A | G | 2 | a0002c0005t0001g0092a0002c0005t0001g0093 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.53+8999A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862196 | ||||||
| chr11:1862232 | A | G | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.53+9035A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862232 | ||||||
| chr11:1862548 | G | A | 1 | a0003c0006t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+9351G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862548 | ||||||
| chr11:1862599 | T | C | 191 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(188): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.53+9402T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862599 | ||||||
| chr11:1862625 | T | C | 190 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(187): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.53+9428T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862625 | ||||||
| chr11:1862709 | C | T | 8 | a0001c0003t0001g0179a0002c0001t0002g0016a0002c0001t0002g0041others(5): Show | 10 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+9512C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862709 | ||||||
| chr11:1862726 | C | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9529C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862726 | ||||||
| chr11:1862727 | ACCTCCCC others(31): Show |
A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9545_53+9582del others(38): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1862727 | |||||
| chr11:1862765 | GCCTCCCC others(12): Show |
G | 186 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(183): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.53+9595_53+9613del others(19): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1862765 | |||||
| chr11:1862771 | CCTGGGTG others(50): Show |
C | 1 | a0002c0001t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.53+9583_53+9639del others(57): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1862771 | |||||
| chr11:1862774 | G | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9577G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862774 | ||||||
| chr11:1862778 | G | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9581G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862778 | ||||||
| chr11:1862784 | A | G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9587A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862784 | ||||||
| chr11:1862849 | T | C | 1 | a0003c0004t0001g0036 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.53+9652T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1862849 | ||||||
| chr11:1863112 | G | A | 111 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(108): Show | 153 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.53+9915G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863112 | ||||||
| chr11:1863123 | G | A | 27 | a0001c0003t0001g0270a0002c0001t0001g0009a0002c0001t0001g0201others(24): Show | 30 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.53+9926G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863123 | ||||||
| chr11:1863133 | ACCACCTG others(11): Show |
A | 5 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+9939_53+9956del others(18): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1863133 | |||||
| chr11:1863181 | C | T | 1 | a0001c0002t0001g0139 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.53+9984C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863181 | ||||||
| chr11:1863215 | C | T | 1 | a0003c0004t0001g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.53+10018C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863215 | ||||||
| chr11:1863637 | A | G | 3 | a0003c0004t0001g0236a0003c0004t0001g0237a0003c0004t0001g0238 | 3 | HG02155.hp1 HG02165.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.53+10440A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863637 | ||||||
| chr11:1863781 | G | A | 1 | a0003c0004t0001g0204 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.53+10584G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863781 | ||||||
| chr11:1863795 | C | G | 208 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(205): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.53+10598C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863795 | ||||||
| chr11:1863796 | A | T | 16 | a0001c0003t0001g0019a0002c0001t0001g0012a0002c0001t0001g0017others(13): Show | 23 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.53+10599A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863796 | ||||||
| chr11:1863883 | G | A | 1 | a0005c0009t0001g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.53+10686G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863883 | ||||||
| chr11:1863887 | A | T | 186 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(183): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.53+10690A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863887 | ||||||
| chr11:1863958 | G | A | 1 | a0002c0005t0001g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.53+10761G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863958 | ||||||
| chr11:1863959 | G | T | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53+10762G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863959 | ||||||
| chr11:1863995 | C | T | 23 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(20): Show | 28 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.53+10798C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1863995 | ||||||
| chr11:1864179 | G | A | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.53+10982G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864179 | ||||||
| chr11:1864307 | G | A | 1 | a0002c0001t0001g0216 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.53+11110G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864307 | ||||||
| chr11:1864354 | C | T | 1 | a0003c0004t0001g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.53+11157C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864354 | ||||||
| chr11:1864373 | C | T | 1 | a0002c0017t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53+11176C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864373 | ||||||
| chr11:1864383 | G | A | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.53+11186G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864383 | ||||||
| chr11:1864414 | C | G | 1 | a0002c0001t0001g0021 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53+11217C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864414 | ||||||
| chr11:1864485 | G | A | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG01358.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.53+11288G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864485 | ||||||
| chr11:1864745 | C | G | 2 | a0001c0002t0001g0104a0001c0002t0001g0138 | 2 | NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.53+11548C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864745 | ||||||
| chr11:1864874 | G | A | 1 | a0003c0006t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+11677G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864874 | ||||||
| chr11:1864917 | G | A | 229 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(226): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.53+11720G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1864917 | ||||||
| chr11:1865013 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.53+11816C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865013 | ||||||
| chr11:1865076 | C | T | 117 | a0001c0002t0001g0200a0001c0003t0001g0007a0001c0003t0001g0037others(114): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.53+11879C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865076 | ||||||
| chr11:1865213 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+12016C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865213 | ||||||
| chr11:1865333 | C | T | 1 | a0002c0005t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53+12136C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865333 | ||||||
| chr11:1865360 | G | A | 1 | a0003c0004t0001g0236 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.53+12163G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865360 | ||||||
| chr11:1865430 | C | T | 6 | a0002c0001t0001g0084a0002c0005t0001g0090a0002c0005t0001g0091others(3): Show | 6 | HG02602.hp1 HG02698.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+12233C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865430 | ||||||
| chr11:1865446 | CCT | C | 50 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(47): Show | 55 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.53+12254_53+12255d others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1865446 | |||||
| chr11:1865456 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.53+12259T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865456 | ||||||
| chr11:1865466 | T | C | 1 | a0002c0001t0006g0245 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.53+12269T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865466 | ||||||
| chr11:1865498 | C | T | 1 | a0001c0002t0001g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.53+12301C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865498 | ||||||
| chr11:1865511 | C | T | 2 | a0002c0001t0002g0176a0002c0001t0002g0180 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.53+12314C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865511 | ||||||
| chr11:1865518 | G | A | 1 | a0003c0004t0001g0178 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.53+12321G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865518 | ||||||
| chr11:1865545 | C | T | 51 | a0001c0002t0001g0200a0001c0003t0001g0285a0002c0001t0001g0008others(48): Show | 56 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.53+12348C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865545 | ||||||
| chr11:1865579 | G | A | 1 | a0003c0004t0001g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53+12382G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865579 | ||||||
| chr11:1865635 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.53+12438A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865635 | ||||||
| chr11:1865660 | G | A | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+12463G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865660 | ||||||
| chr11:1865711 | C | T | 1 | a0002c0005t0001g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.53+12514C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865711 | ||||||
| chr11:1865712 | G | A | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+12515G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865712 | ||||||
| chr11:1865748 | A | G | 72 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(69): Show | 89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.53+12551A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865748 | ||||||
| chr11:1865749 | A | T | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+12552A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865749 | ||||||
| chr11:1865777 | T | A | 1 | a0001c0002t0001g0135 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.53+12580T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865777 | ||||||
| chr11:1865838 | T | G | 131 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(128): Show | 173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.53+12641T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865838 | ||||||
| chr11:1865927 | C | T | 51 | a0001c0002t0001g0200a0001c0003t0001g0285a0002c0001t0001g0008others(48): Show | 56 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.53+12730C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865927 | ||||||
| chr11:1865986 | T | C | 169 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(166): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.53+12789T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1865986 | ||||||
| chr11:1866067 | C | A | 1 | a0004c0008t0001g0164 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.53+12870C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866067 | ||||||
| chr11:1866068 | C | G | 1 | a0004c0008t0001g0164 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.53+12871C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866068 | ||||||
| chr11:1866117 | G | A | 1 | a0002c0017t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53+12920G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866117 | ||||||
| chr11:1866143 | T | A | 1 | a0001c0003t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.53+12946T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866143 | ||||||
| chr11:1866217 | T | C | 1 | a0001c0003t0001g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.53+13020T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866217 | ||||||
| chr11:1866288 | G | A | 18 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(15): Show | 27 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.53+13091G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866288 | ||||||
| chr11:1866294 | C | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+13097C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866294 | ||||||
| chr11:1866301 | C | T | 48 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(45): Show | 53 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.53+13104C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866301 | ||||||
| chr11:1866381 | G | C | 1 | a0001c0003t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.53+13184G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866381 | ||||||
| chr11:1866405 | G | C | 1 | a0002c0001t0001g0215 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53+13208G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866405 | ||||||
| chr11:1866428 | C | T | 1 | a0003c0004t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.53+13231C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866428 | ||||||
| chr11:1866446 | A | C | 1 | a0002c0005t0001g0130 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.53+13249A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866446 | ||||||
| chr11:1866458 | C | T | 1 | a0001c0003t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.53+13261C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866458 | ||||||
| chr11:1866533 | C | G | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+13336C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866533 | ||||||
| chr11:1866538 | C | T | 1 | a0002c0016t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.53+13341C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866538 | ||||||
| chr11:1866576 | T | A | 184 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(181): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.53+13379T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866576 | ||||||
| chr11:1866777 | G | A | 2 | a0002c0001t0001g0246a0002c0001t0001g0259 | 2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.54-13310G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866777 | ||||||
| chr11:1866799 | C | A | 1 | a0002c0001t0001g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.54-13288C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866799 | ||||||
| chr11:1866802 | C | T | 1 | a0001c0002t0001g0025 | 2 | NA18944.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.54-13285C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1866802 | ||||||
| chr11:1867003 | C | G | 2 | a0002c0001t0001g0244a0002c0001t0001g0253 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-13084C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867003 | ||||||
| chr11:1867018 | AGGGCCAG others(50): Show |
A | 1 | a0001c0002t0001g0109 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.54-13039_54-12983d others(59): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1867018 | |||||
| chr11:1867045 | G | A | 4 | a0003c0004t0001g0208a0003c0004t0001g0209a0003c0004t0001g0210others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-13042G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867045 | ||||||
| chr11:1867061 | G | A | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-13026G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867061 | ||||||
| chr11:1867111 | A | G | 222 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(219): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.54-12976A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867111 | ||||||
| chr11:1867362 | C | T | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-12725C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867362 | ||||||
| chr11:1867384 | C | T | 104 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(101): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.54-12703C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867384 | ||||||
| chr11:1867385 | G | T | 1 | a0001c0002t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.54-12702G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867385 | ||||||
| chr11:1867658 | G | C | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-12429G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867658 | ||||||
| chr11:1867725 | G | A | 26 | a0001c0003t0001g0258a0001c0003t0001g0265a0002c0001t0001g0006others(23): Show | 29 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.54-12362G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867725 | ||||||
| chr11:1867823 | G | A | 2 | a0001c0003t0001g0048a0001c0003t0001g0069 | 2 | NA19005.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.54-12264G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867823 | ||||||
| chr11:1867826 | G | A | 1 | a0002c0001t0001g0080 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.54-12261G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867826 | ||||||
| chr11:1867846 | C | T | 2 | a0001c0003t0001g0055a0001c0003t0001g0072 | 2 | HG00099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.54-12241C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867846 | ||||||
| chr11:1867872 | A | G | 227 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(224): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.54-12215A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1867872 | ||||||
| chr11:1868003 | G | A | 1 | a0004c0008t0001g0164 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54-12084G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868003 | ||||||
| chr11:1868019 | C | T | 131 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(128): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.54-12068C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868019 | ||||||
| chr11:1868057 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.54-12030C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868057 | ||||||
| chr11:1868164 | G | A | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.54-11923G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868164 | ||||||
| chr11:1868176 | C | T | 25 | a0001c0003t0001g0258a0001c0003t0001g0265a0002c0001t0001g0006others(22): Show | 28 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-11911C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868176 | ||||||
| chr11:1868429 | G | A | 1 | a0001c0003t0001g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.54-11658G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868429 | ||||||
| chr11:1868442 | C | T | 13 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(10): Show | 16 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-11645C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868442 | ||||||
| chr11:1868846 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-11241C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868846 | ||||||
| chr11:1868857 | C | T | 1 | a0001c0002t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.54-11230C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868857 | ||||||
| chr11:1868975 | G | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-11112G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1868975 | ||||||
| chr11:1869091 | C | T | 70 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(67): Show | 80 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.54-10996C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869091 | ||||||
| chr11:1869157 | C | T | 1 | a0002c0001t0001g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.54-10930C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869157 | ||||||
| chr11:1869203 | A | G | 1 | a0001c0003t0001g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.54-10884A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869203 | ||||||
| chr11:1869230 | G | A | 13 | a0001c0002t0001g0002a0001c0002t0001g0096a0001c0002t0001g0107others(10): Show | 19 | HG00621.hp2 HG01258.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.54-10857G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869230 | ||||||
| chr11:1869341 | A | G | 20 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(17): Show | 29 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.54-10746A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869341 | ||||||
| chr11:1869496 | A | C | 1 | a0002c0001t0001g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-10591A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869496 | ||||||
| chr11:1869501 | G | C | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.54-10586G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869501 | ||||||
| chr11:1869513 | C | T | 2 | a0001c0003t0001g0055a0001c0003t0001g0072 | 2 | HG00099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.54-10574C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869513 | ||||||
| chr11:1869557 | C | T | 1 | a0002c0001t0001g0267 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54-10530C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869557 | ||||||
| chr11:1869580 | G | A | 216 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(213): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.54-10507G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869580 | ||||||
| chr11:1869591 | G | A | 25 | a0001c0003t0001g0258a0001c0003t0001g0265a0002c0001t0001g0006others(22): Show | 28 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-10496G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869591 | ||||||
| chr11:1869599 | C | A | 25 | a0001c0003t0001g0258a0001c0003t0001g0265a0002c0001t0001g0006others(22): Show | 28 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-10488C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869599 | ||||||
| chr11:1869611 | G | GC | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-10474dupC | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1869611 | |||||
| chr11:1869614 | G | C | 15 | a0002c0005t0001g0086a0003c0004t0001g0032a0003c0004t0001g0036others(12): Show | 17 | HG00642.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-10473G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869614 | ||||||
| chr11:1869653 | TGGTGCTC others(7): Show |
T | 13 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(10): Show | 16 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-10431_54-10418d others(16): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1869653 | |||||
| chr11:1869741 | C | A | 44 | a0002c0001t0001g0215a0002c0001t0001g0216a0002c0001t0001g0223others(41): Show | 48 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.54-10346C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869741 | ||||||
| chr11:1869760 | G | A | 162 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(159): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.54-10327G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869760 | ||||||
| chr11:1869805 | G | GA | 290 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(287): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.54-10282_54-10281i others(3): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869805 | ||||||
| chr11:1869811 | G | T | 1 | a0001c0003t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.54-10276G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869811 | ||||||
| chr11:1869847 | C | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-10240C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869847 | ||||||
| chr11:1869974 | C | T | 1 | a0003c0004t0001g0233 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.54-10113C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1869974 | ||||||
| chr11:1870007 | G | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-10080G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870007 | ||||||
| chr11:1870011 | G | A | 24 | a0001c0003t0001g0265a0002c0001t0001g0006a0002c0001t0001g0035others(21): Show | 27 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.54-10076G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870011 | ||||||
| chr11:1870026 | G | A | 1 | a0002c0005t0001g0118 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.54-10061G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870026 | ||||||
| chr11:1870054 | T | A | 203 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(200): Show | 255 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.54-10033T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870054 | ||||||
| chr11:1870089 | C | T | 30 | a0002c0001t0001g0084a0002c0001t0001g0202a0002c0001t0001g0235others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.54-9998C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870089 | ||||||
| chr11:1870095 | C | T | 12 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0151others(9): Show | 15 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.54-9992C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870095 | ||||||
| chr11:1870205 | C | T | 1 | a0002c0001t0001g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.54-9882C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870205 | ||||||
| chr11:1870273 | G | C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-9814G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870273 | ||||||
| chr11:1870357 | C | T | 2 | a0002c0001t0001g0262a0002c0001t0001g0263 | 2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.54-9730C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870357 | ||||||
| chr11:1870369 | A | C | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-9718A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870369 | ||||||
| chr11:1870369 | A | T | 17 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(14): Show | 20 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.54-9718A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870369 | ||||||
| chr11:1870492 | C | T | 106 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(103): Show | 145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.54-9595C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870492 | ||||||
| chr11:1870656 | G | A | 24 | a0001c0003t0001g0265a0002c0001t0001g0006a0002c0001t0001g0035others(21): Show | 27 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.54-9431G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870656 | ||||||
| chr11:1870661 | G | C | 1 | a0003c0004t0002g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.54-9426G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870661 | ||||||
| chr11:1870675 | C | G | 72 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(69): Show | 82 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.54-9412C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870675 | ||||||
| chr11:1870718 | G | A | 16 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(13): Show | 19 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-9369G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870718 | ||||||
| chr11:1870722 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.54-9365C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870722 | ||||||
| chr11:1870723 | G | A | 18 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(15): Show | 27 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.54-9364G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870723 | ||||||
| chr11:1870744 | A | C | 22 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(19): Show | 27 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.54-9343A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870744 | ||||||
| chr11:1870872 | G | C | 2 | a0003c0004t0001g0241a0003c0004t0001g0242 | 2 | HG00642.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.54-9215G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870872 | ||||||
| chr11:1870912 | C | T | 1 | a0002c0005t0001g0133 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.54-9175C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870912 | ||||||
| chr11:1870931 | G | A | 3 | a0002c0001t0001g0267a0002c0001t0001g0280a0002c0001t0005g0266 | 3 | HG00323.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.54-9156G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1870931 | ||||||
| chr11:1871070 | C | T | 3 | a0002c0001t0001g0215a0003c0004t0001g0178a0003c0004t0001g0232 | 3 | HG00323.hp2 HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.54-9017C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871070 | ||||||
| chr11:1871113 | A | G | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-8974A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871113 | ||||||
| chr11:1871155 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.54-8932A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871155 | ||||||
| chr11:1871255 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.54-8832C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871255 | ||||||
| chr11:1871294 | G | C | 6 | a0002c0005t0001g0013a0002c0005t0001g0097a0002c0005t0001g0118others(3): Show | 7 | HG00558.hp2 HG02027.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-8793G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871294 | ||||||
| chr11:1871332 | G | T | 7 | a0001c0003t0001g0285a0002c0001t0001g0029a0002c0001t0001g0075others(4): Show | 8 | HG02132.hp1 HG04115.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-8755G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871332 | ||||||
| chr11:1871355 | G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(127): Show | 172 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.54-8732G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871355 | ||||||
| chr11:1871483 | T | A | 1 | a0003c0004t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.54-8604T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871483 | ||||||
| chr11:1871489 | C | T | 1 | a0002c0005t0009g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54-8598C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871489 | ||||||
| chr11:1871542 | G | T | 1 | a0002c0005t0001g0133 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.54-8545G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871542 | ||||||
| chr11:1871545 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.54-8542G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871545 | ||||||
| chr11:1871663 | C | T | 1 | a0003c0004t0001g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.54-8424C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871663 | ||||||
| chr11:1871700 | G | A | 105 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(102): Show | 144 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.54-8387G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871700 | ||||||
| chr11:1871716 | G | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-8371G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871716 | ||||||
| chr11:1871734 | A | AG | 8 | a0001c0002t0001g0136a0001c0003t0001g0040a0001c0003t0001g0049others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-8347dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871734 | |||||
| chr11:1871741 | T | TGTGTGTG others(557): Show |
1 | a0002c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.54-8214_54-8213ins others(564): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871741 | |||||
| chr11:1871777 | A | G | 1 | a0002c0001t0001g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-8310A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871777 | ||||||
| chr11:1871783 | TGCTGGTA others(87): Show |
T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8281_54-8188del others(94): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871783 | |||||
| chr11:1871806 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-8281C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871806 | ||||||
| chr11:1871830 | C | A | 1 | a0007c0015t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-8257C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871830 | ||||||
| chr11:1871830 | C | CG | 4 | a0002c0001t0001g0080a0002c0001t0001g0246a0002c0001t0001g0248others(1): Show | 4 | HG00544.hp2 HG03942.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8253dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871830 | |||||
| chr11:1871845 | A | AGGCAGGC others(369): Show |
1 | a0003c0004t0001g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.54-8214_54-8213ins others(376): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871845 | |||||
| chr11:1871874 | G | A | 102 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(99): Show | 112 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.54-8213G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871874 | ||||||
| chr11:1871877 | C | T | 50 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(47): Show | 55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.54-8210C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1871877 | ||||||
| chr11:1871923 | A | AG | 22 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0121others(19): Show | 22 | HG00438.hp1 HG00544.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.54-8157dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1871923 | |||||
| chr11:1872023 | T | G | 1 | a0001c0003t0001g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54-8064T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872023 | ||||||
| chr11:1872048 | A | G | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-8039A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872048 | ||||||
| chr11:1872096 | G | A | 1 | a0002c0001t0001g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.54-7991G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872096 | ||||||
| chr11:1872111 | A | AG | 6 | a0001c0002t0001g0105a0001c0003t0001g0070a0001c0003t0001g0270others(3): Show | 6 | HG00544.hp1 HG01175.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-7971dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872111 | |||||
| chr11:1872112 | GGGGGTGT others(87): Show |
G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-7961_54-7868del others(94): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872112 | |||||
| chr11:1872127 | G | A | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-7960G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872127 | ||||||
| chr11:1872198 | C | T | 1 | a0002c0001t0002g0020 | 2 | HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.54-7889C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872198 | ||||||
| chr11:1872206 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-7881C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872206 | ||||||
| chr11:1872210 | G | T | 14 | a0001c0003t0001g0004a0001c0003t0001g0010a0001c0003t0001g0042others(11): Show | 20 | HG00423.hp1 HG01175.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.54-7877G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872210 | ||||||
| chr11:1872276 | C | T | 101 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(98): Show | 111 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.54-7811C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872276 | ||||||
| chr11:1872286 | G | GGGCACTT others(88): Show |
1 | a0002c0001t0001g0272 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.54-7796_54-7795ins others(95): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872286 | |||||
| chr11:1872286 | G | GGGCACTT others(88): Show |
1 | a0002c0001t0001g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.54-7796_54-7795ins others(95): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872286 | |||||
| chr11:1872286 | G | GGGCACTT others(87): Show |
99 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(96): Show | 109 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.54-7796_54-7795ins others(94): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872286 | |||||
| chr11:1872308 | C | G | 10 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(7): Show | 12 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-7779C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872308 | ||||||
| chr11:1872314 | T | C | 256 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(253): Show | 313 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.54-7773T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872314 | ||||||
| chr11:1872368 | T | G | 1 | a0003c0004t0001g0233 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.54-7719T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872368 | ||||||
| chr11:1872394 | C | T | 30 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0235others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.54-7693C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872394 | ||||||
| chr11:1872425 | C | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-7662C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872425 | ||||||
| chr11:1872469 | G | C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-7618G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872469 | ||||||
| chr11:1872471 | G | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-7616G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872471 | ||||||
| chr11:1872502 | GGGCAGGC others(87): Show |
G | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-7569_54-7476del others(94): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872502 | |||||
| chr11:1872534 | C | T | 2 | a0002c0001t0001g0077a0002c0001t0001g0078 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.54-7553C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872534 | ||||||
| chr11:1872570 | C | A | 1 | a0002c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-7517C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872570 | ||||||
| chr11:1872580 | A | AG | 8 | a0001c0002t0001g0113a0001c0003t0001g0037a0001c0003t0001g0270others(5): Show | 8 | HG00544.hp2 HG00621.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-7502dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872580 | |||||
| chr11:1872621 | C | T | 113 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(110): Show | 125 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.54-7466C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872621 | ||||||
| chr11:1872674 | A | AG | 7 | a0001c0002t0001g0094a0001c0003t0001g0040a0002c0001t0001g0254others(4): Show | 7 | HG00741.hp2 HG01099.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-7408dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1872674 | |||||
| chr11:1872689 | C | T | 19 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(16): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.54-7398C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872689 | ||||||
| chr11:1872752 | C | T | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.54-7335C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872752 | ||||||
| chr11:1872809 | C | T | 2 | a0002c0001t0001g0262a0002c0001t0001g0263 | 2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.54-7278C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872809 | ||||||
| chr11:1872925 | A | G | 1 | a0001c0003t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.54-7162A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872925 | ||||||
| chr11:1872933 | A | G | 101 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(98): Show | 111 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.54-7154A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1872933 | ||||||
| chr11:1873002 | C | T | 275 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(272): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.54-7085C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873002 | ||||||
| chr11:1873074 | G | T | 1 | a0002c0005t0001g0133 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.54-7013G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873074 | ||||||
| chr11:1873234 | A | T | 1 | a0001c0003t0001g0049 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.54-6853A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873234 | ||||||
| chr11:1873310 | C | T | 1 | a0001c0003t0001g0270 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.54-6777C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873310 | ||||||
| chr11:1873500 | T | TGGAG | 105 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(102): Show | 144 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.54-6565_54-6562dup others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873500 | |||||
| chr11:1873500 | TGGAG | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6565_54-6562del others(4): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873500 | |||||
| chr11:1873574 | A | G | 275 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(272): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.54-6513A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873574 | ||||||
| chr11:1873584 | A | C | 26 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(23): Show | 33 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.54-6503A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873584 | ||||||
| chr11:1873627 | AAGG | A | 19 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(16): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.54-6457_54-6455del others(3): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873627 | |||||
| chr11:1873719 | T | A | 1 | a0002c0001t0001g0281 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.54-6368T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873719 | ||||||
| chr11:1873810 | C | G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6277C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873810 | ||||||
| chr11:1873810 | CCCAGCAG others(27): Show |
C | 3 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175 | 3 | HG00735.hp1 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.54-6274_54-6241del others(34): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873810 | |||||
| chr11:1873813 | A | G | 112 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(109): Show | 123 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.54-6274A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873813 | ||||||
| chr11:1873813 | AGCAGAGG others(10): Show |
A | 2 | a0002c0001t0001g0018a0002c0001t0001g0076 | 3 | HG00438.hp2 NA18946.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.54-6241_54-6225del others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873813 | |||||
| chr11:1873837 | GAGGGAGG others(163): Show |
G | 4 | a0002c0001t0002g0016a0002c0001t0002g0176a0002c0001t0002g0177others(1): Show | 5 | HG00280.hp2 HG01070.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-6224_54-6055del | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873837 | |||||
| chr11:1873844 | G | GCCGGCAG others(10): Show |
73 | a0001c0002t0001g0200a0001c0003t0001g0258a0002c0001t0001g0201others(70): Show | 77 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.54-6234_54-6233ins others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873844 | |||||
| chr11:1873844 | G | GCCGGCAG others(129): Show |
1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-6234_54-6233ins others(136): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873844 | |||||
| chr11:1873850 | A | AGAGCAGG others(78): Show |
4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6234_54-6233ins others(85): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873850 | |||||
| chr11:1873854 | G | C | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-6233G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873854 | ||||||
| chr11:1873863 | T | C | 97 | a0001c0002t0001g0200a0001c0003t0001g0258a0001c0003t0001g0285others(94): Show | 106 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.54-6224T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873863 | ||||||
| chr11:1873863 | T | TGGCAGAG others(180): Show |
8 | a0002c0001t0001g0215a0003c0004t0001g0034a0003c0004t0001g0178others(5): Show | 9 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-6217_54-6216ins others(187): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873863 | |||||
| chr11:1873867 | A | G | 1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-6220A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873867 | ||||||
| chr11:1873871 | G | C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6216G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873871 | ||||||
| chr11:1873871 | GAGGGAGG others(10): Show |
G | 1 | a0002c0005t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.54-6209_54-6193del others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873871 | |||||
| chr11:1873871 | GAGGGAGG others(129): Show |
G | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-6207_54-6072del | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873871 | |||||
| chr11:1873880 | T | C | 12 | a0002c0001t0001g0215a0003c0004t0001g0034a0003c0004t0001g0178others(9): Show | 13 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-6207T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873880 | ||||||
| chr11:1873888 | C | G | 12 | a0002c0001t0001g0215a0003c0004t0001g0034a0003c0004t0001g0178others(9): Show | 13 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-6199C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873888 | ||||||
| chr11:1873888 | CAGGGAGC others(129): Show |
C | 3 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175 | 3 | HG00735.hp1 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.54-6192_54-6057del | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873888 | |||||
| chr11:1873895 | C | G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6192C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873895 | ||||||
| chr11:1873918 | G | GGAGGAGG others(27): Show |
1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-6153_54-6152ins others(34): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873918 | |||||
| chr11:1873931 | C | CGGCAGAG others(61): Show |
3 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.54-6142_54-6141ins others(68): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873931 | |||||
| chr11:1873935 | A | G | 8 | a0002c0001t0001g0215a0003c0004t0001g0034a0003c0004t0001g0178others(5): Show | 9 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-6152A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873935 | ||||||
| chr11:1873948 | C | CGGCAGAG others(265): Show |
1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54-6119_54-6118ins others(272): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873948 | |||||
| chr11:1873948 | C | T | 6 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-6139C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873948 | ||||||
| chr11:1873952 | A | G | 1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-6135A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873952 | ||||||
| chr11:1873969 | G | A | 88 | a0001c0002t0001g0200a0001c0003t0001g0258a0002c0001t0001g0201others(85): Show | 93 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.54-6118G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873969 | ||||||
| chr11:1873969 | G | GGAGGAGG others(61): Show |
1 | a0002c0001t0001g0081 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.54-6089_54-6088ins others(68): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873969 | |||||
| chr11:1873969 | G | GGAGGAGG others(44): Show |
1 | a0002c0001t0001g0021 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.54-6074_54-6073ins others(51): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873969 | |||||
| chr11:1873969 | G | GGAGGAGG others(44): Show |
54 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0025others(51): Show | 68 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.54-6074_54-6073ins others(51): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873969 | |||||
| chr11:1873969 | G | GGAGGAGG others(163): Show |
1 | a0002c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.54-6074_54-6073ins others(170): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873969 | |||||
| chr11:1873969 | G | GGAGGAGG others(95): Show |
2 | a0002c0005t0001g0027a0002c0005t0001g0151 | 3 | HG00639.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.54-6023_54-6022ins others(102): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873969 | |||||
| chr11:1873973 | G | GAGGGAGG others(78): Show |
3 | a0002c0001t0001g0009a0002c0001t0001g0017a0002c0001t0001g0280 | 5 | HG01081.hp1 HG01515.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-6074_54-6073ins others(85): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873973 | |||||
| chr11:1873974 | A | AGGGAGGC others(45): Show |
1 | a0002c0005t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-6074_54-6073ins others(52): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873974 | |||||
| chr11:1873986 | G | A | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-6101G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873986 | ||||||
| chr11:1873999 | T | C | 43 | a0001c0003t0001g0258a0002c0001t0001g0216a0002c0001t0001g0223others(40): Show | 47 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.54-6088T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1873999 | ||||||
| chr11:1873999 | T | TGGCAGAG others(163): Show |
28 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0235others(25): Show | 28 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-6074_54-6073ins others(170): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873999 | |||||
| chr11:1873999 | T | TGGCAGAG others(10): Show |
1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-6080_54-6064dup others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873999 | |||||
| chr11:1873999 | T | TGGCGGAG others(61): Show |
1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-6085_54-6084ins others(68): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1873999 | |||||
| chr11:1874014 | G | C | 162 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(159): Show | 195 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.54-6073G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874014 | ||||||
| chr11:1874016 | C | T | 4 | a0002c0001t0002g0016a0002c0001t0002g0176a0002c0001t0002g0177others(1): Show | 5 | HG00280.hp2 HG01070.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-6071C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874016 | ||||||
| chr11:1874024 | G | C | 24 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(21): Show | 30 | HG00280.hp2 HG01070.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.54-6063G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874024 | ||||||
| chr11:1874037 | A | G | 162 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(159): Show | 195 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.54-6050A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874037 | ||||||
| chr11:1874041 | G | C | 30 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0235others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.54-6046G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874041 | ||||||
| chr11:1874041 | G | GAGGGAGG others(10): Show |
1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54-6038_54-6037ins others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874041 | |||||
| chr11:1874050 | T | C | 84 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0025others(81): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.54-6037T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874050 | ||||||
| chr11:1874054 | A | G | 2 | a0003c0004t0001g0221a0003c0006t0001g0152 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.54-6033A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874054 | ||||||
| chr11:1874058 | C | CAGGGAGG others(10): Show |
4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6012_54-5996dup others(17): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874058 | |||||
| chr11:1874065 | G | C | 63 | a0001c0003t0001g0258a0001c0003t0001g0285a0002c0001t0001g0008others(60): Show | 72 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.54-6022G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874065 | ||||||
| chr11:1874071 | A | AGAGGAGG others(44): Show |
2 | a0001c0002t0001g0003a0001c0002t0001g0131 | 2 | HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.54-5996_54-5995ins others(51): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874071 | |||||
| chr11:1874071 | A | G | 97 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0025others(94): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.54-6016A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874071 | ||||||
| chr11:1874084 | C | T | 30 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0009others(27): Show | 37 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.54-6003C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874084 | ||||||
| chr11:1874085 | GGCAGAGC others(1): Show |
G | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-6000_54-5993del others(8): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874085 | |||||
| chr11:1874092 | C | G | 153 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(150): Show | 185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.54-5995C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874092 | ||||||
| chr11:1874094 | G | A | 9 | a0001c0002t0001g0003a0001c0002t0001g0088a0001c0002t0001g0094others(6): Show | 14 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-5993G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874094 | ||||||
| chr11:1874097 | AGGCCGG | A | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5989_54-5984del others(6): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874097 | ||||||
| chr11:1874099 | G | C | 49 | a0001c0003t0001g0258a0002c0001t0001g0216a0002c0001t0001g0223others(46): Show | 55 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.54-5988G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874099 | ||||||
| chr11:1874101 | C | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5986C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874101 | ||||||
| chr11:1874107 | A | T | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5980A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874107 | ||||||
| chr11:1874109 | G | C | 140 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(137): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.54-5978G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874109 | ||||||
| chr11:1874110 | A | G | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5977A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874110 | ||||||
| chr11:1874113 | G | C | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5974G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874113 | ||||||
| chr11:1874113 | G | GAGGCCGG others(98): Show |
4 | a0002c0001t0001g0009a0002c0001t0001g0017a0002c0001t0001g0281others(1): Show | 4 | HG00733.hp1 HG01168.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5970_54-5969ins others(105): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874113 | |||||
| chr11:1874113 | G | GAGGCCGG others(63): Show |
1 | a0001c0003t0001g0056 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.54-5970_54-5969ins others(70): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874113 | |||||
| chr11:1874113 | G | GAGGCCGG others(64): Show |
98 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(95): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.54-5970_54-5969ins others(71): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874113 | |||||
| chr11:1874113 | G | GAGGCCGG others(65): Show |
1 | a0002c0001t0001g0246 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.54-5970_54-5969ins others(72): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874113 | |||||
| chr11:1874118 | T | C | 169 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(166): Show | 205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.54-5969T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874118 | ||||||
| chr11:1874120 | G | GC | 43 | a0001c0003t0001g0258a0002c0001t0001g0216a0002c0001t0001g0223others(40): Show | 47 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.54-5967_54-5966ins others(1): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874120 | ||||||
| chr11:1874120 | G | GCAGAGCA others(41): Show |
8 | a0002c0001t0001g0215a0003c0004t0001g0034a0003c0004t0001g0178others(5): Show | 9 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-5967_54-5966ins others(48): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874120 | ||||||
| chr11:1874121 | G | A | 124 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(121): Show | 156 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.54-5966G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874121 | ||||||
| chr11:1874121 | G | C | 10 | a0002c0001t0001g0215a0002c0005t0001g0099a0002c0016t0001g0098others(7): Show | 11 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-5966G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874121 | ||||||
| chr11:1874121 | G | GGACAGTG others(13): Show |
67 | a0001c0002t0001g0003a0001c0002t0001g0005a0001c0002t0001g0023others(64): Show | 85 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-5947_54-5946ins others(20): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874121 | |||||
| chr11:1874123 | A | AGGAGGGA others(244): Show |
3 | a0002c0005t0001g0086a0002c0005t0009g0085a0003c0006t0001g0087 | 3 | HG01884.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.54-5964_54-5963ins others(251): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874123 | A | AGGAGGGA others(244): Show |
29 | a0001c0003t0001g0258a0002c0001t0001g0216a0002c0001t0001g0223others(26): Show | 31 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.54-5964_54-5963ins others(251): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874123 | A | AGGAGGGA others(244): Show |
1 | a0003c0004t0001g0036 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.54-5964_54-5963ins others(251): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874123 | A | AGGAGGGA others(244): Show |
4 | a0003c0004t0001g0208a0003c0004t0001g0209a0003c0004t0001g0210others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-5964_54-5963ins others(251): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874123 | A | AGGAGGGA others(244): Show |
6 | a0003c0004t0001g0032a0003c0004t0001g0213a0003c0004t0001g0220others(3): Show | 7 | HG01070.hp2 HG01109.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.54-5964_54-5963ins others(251): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874123 | A | G | 10 | a0002c0001t0001g0215a0002c0005t0001g0099a0002c0016t0001g0098others(7): Show | 11 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-5964A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874123 | ||||||
| chr11:1874124 | C | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5963C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874124 | ||||||
| chr11:1874125 | A | G | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5962A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874125 | ||||||
| chr11:1874127 | T | A | 53 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(50): Show | 58 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.54-5960T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874127 | ||||||
| chr11:1874130 | G | A | 51 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(48): Show | 56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.54-5957G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874130 | ||||||
| chr11:1874133 | C | G | 51 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(48): Show | 56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.54-5954C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874133 | ||||||
| chr11:1874136 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5951G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874136 | ||||||
| chr11:1874137 | C | G | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5950C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874137 | ||||||
| chr11:1874138 | C | T | 51 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(48): Show | 56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.54-5949C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874138 | ||||||
| chr11:1874139 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5948G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874139 | ||||||
| chr11:1874141 | G | A | 10 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(7): Show | 12 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5946G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874141 | ||||||
| chr11:1874141 | G | GGACAGTG others(13): Show |
30 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0235others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.54-5927_54-5926ins others(20): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874141 | |||||
| chr11:1874147 | T | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5940T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874147 | ||||||
| chr11:1874150 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5937G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874150 | ||||||
| chr11:1874153 | C | G | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5934C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874153 | ||||||
| chr11:1874158 | C | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5929C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874158 | ||||||
| chr11:1874161 | G | A | 55 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(52): Show | 60 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.54-5926G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874161 | ||||||
| chr11:1874162 | G | C | 1 | a0001c0003t0001g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.54-5925G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874162 | ||||||
| chr11:1874169 | GGAGCAGT others(55): Show |
G | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5916_54-5855del others(62): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874169 | |||||
| chr11:1874171 | A | G | 57 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(54): Show | 62 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.54-5916A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874171 | ||||||
| chr11:1874175 | GT | G | 57 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(54): Show | 62 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.54-5911delT | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874175 | ||||||
| chr11:1874178 | T | C | 57 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(54): Show | 62 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.54-5909T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874178 | ||||||
| chr11:1874182 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5905G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874182 | ||||||
| chr11:1874199 | T | C | 57 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(54): Show | 62 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.54-5888T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874199 | ||||||
| chr11:1874208 | TGGGGGCA others(73): Show |
T | 20 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(17): Show | 25 | HG01243.hp2 HG01433.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5809_54-5730del others(80): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874208 | |||||
| chr11:1874212 | G | A | 55 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(52): Show | 60 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.54-5875G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874212 | ||||||
| chr11:1874219 | T | C | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5868T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874219 | ||||||
| chr11:1874220 | T | C | 57 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(54): Show | 62 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.54-5867T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874220 | ||||||
| chr11:1874231 | A | G | 6 | a0002c0005t0001g0099a0002c0016t0001g0098a0003c0004t0001g0195others(3): Show | 6 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-5856A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874231 | ||||||
| chr11:1874233 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5854G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874233 | ||||||
| chr11:1874239 | C | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-5848C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874239 | ||||||
| chr11:1874240 | C | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5847C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874240 | ||||||
| chr11:1874251 | G | GGGGCAGT others(14): Show |
4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5830_54-5829ins others(21): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874251 | |||||
| chr11:1874253 | G | A | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5834G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874253 | ||||||
| chr11:1874257 | G | GT | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5830_54-5829ins others(1): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874257 | ||||||
| chr11:1874259 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5828C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874259 | ||||||
| chr11:1874260 | T | C | 10 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(7): Show | 12 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5827T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874260 | ||||||
| chr11:1874260 | T | TGGGGACA others(54): Show |
2 | a0001c0003t0001g0168a0001c0003t0001g0170 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.54-5808_54-5807ins others(61): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874260 | |||||
| chr11:1874280 | C | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5807C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874280 | ||||||
| chr11:1874286 | C | CA | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5801_54-5800ins others(1): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874286 | ||||||
| chr11:1874286 | C | CG | 25 | a0001c0002t0001g0088a0001c0002t0001g0108a0001c0002t0001g0124others(22): Show | 25 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.54-5794dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1874286 | |||||
| chr11:1874288 | G | T | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-5799G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874288 | ||||||
| chr11:1874478 | C | A | 131 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(128): Show | 173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.54-5609C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874478 | ||||||
| chr11:1874488 | T | G | 1 | a0002c0005t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-5599T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874488 | ||||||
| chr11:1874489 | G | T | 1 | a0002c0005t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-5598G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874489 | ||||||
| chr11:1874512 | G | A | 4 | a0001c0002t0001g0026a0001c0002t0001g0136a0001c0002t0001g0139others(1): Show | 5 | HG02074.hp1 NA18951.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-5575G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874512 | ||||||
| chr11:1874544 | T | G | 1 | a0002c0005t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-5543T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874544 | ||||||
| chr11:1874688 | C | T | 59 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(56): Show | 82 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.54-5399C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874688 | ||||||
| chr11:1874730 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.54-5357C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874730 | ||||||
| chr11:1874828 | C | G | 1 | a0001c0002t0001g0135 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.54-5259C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1874828 | ||||||
| chr11:1875042 | C | T | 1 | a0002c0016t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54-5045C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875042 | ||||||
| chr11:1875060 | CCTGGGTC others(143): Show |
C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5023_54-4874del | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1875060 | |||||
| chr11:1875174 | C | T | 19 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(16): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.54-4913C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875174 | ||||||
| chr11:1875281 | T | C | 258 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(255): Show | 315 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.54-4806T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875281 | ||||||
| chr11:1875374 | G | T | 1 | a0002c0001t0001g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.54-4713G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875374 | ||||||
| chr11:1875441 | G | C | 1 | a0002c0001t0001g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-4646G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875441 | ||||||
| chr11:1875547 | T | C | 30 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0235others(27): Show | 30 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.54-4540T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875547 | ||||||
| chr11:1875559 | G | A | 1 | a0002c0001t0002g0020 | 2 | HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.54-4528G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875559 | ||||||
| chr11:1875613 | C | T | 20 | a0001c0003t0001g0066a0002c0001t0001g0009a0002c0001t0001g0012others(17): Show | 29 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.54-4474C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875613 | ||||||
| chr11:1875632 | T | C | 1 | a0002c0005t0001g0118 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.54-4455T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875632 | ||||||
| chr11:1875705 | G | A | 26 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(23): Show | 32 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.54-4382G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875705 | ||||||
| chr11:1875724 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.54-4363C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875724 | ||||||
| chr11:1875725 | G | A | 3 | a0001c0003t0001g0184a0001c0003t0001g0185a0001c0003t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.54-4362G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875725 | ||||||
| chr11:1875727 | G | C | 131 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(128): Show | 173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.54-4360G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875727 | ||||||
| chr11:1875813 | G | A | 1 | a0002c0001t0001g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.54-4274G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875813 | ||||||
| chr11:1875833 | C | T | 2 | a0002c0001t0001g0160a0002c0001t0001g0167 | 2 | HG02132.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.54-4254C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875833 | ||||||
| chr11:1875859 | C | T | 1 | a0003c0004t0003g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.54-4228C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1875859 | ||||||
| chr11:1876060 | C | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54-4027C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876060 | ||||||
| chr11:1876128 | G | A | 1 | a0003c0004t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54-3959G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876128 | ||||||
| chr11:1876210 | C | G | 26 | a0001c0003t0001g0285a0002c0001t0001g0008a0002c0001t0001g0029others(23): Show | 33 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.54-3877C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876210 | ||||||
| chr11:1876444 | C | A | 1 | a0005c0009t0001g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-3643C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876444 | ||||||
| chr11:1876457 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.54-3630G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876457 | ||||||
| chr11:1876552 | G | A | 1 | a0004c0008t0001g0164 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54-3535G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876552 | ||||||
| chr11:1876606 | G | A | 2 | a0002c0001t0002g0016a0002c0001t0002g0041 | 4 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-3481G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876606 | ||||||
| chr11:1876738 | AAGG | A | 64 | a0001c0002t0001g0022a0001c0002t0001g0104a0001c0002t0001g0125others(61): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.54-3346_54-3344del others(3): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1876738 | |||||
| chr11:1876741 | GAGA | G | 47 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(44): Show | 52 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.54-3340_54-3338del others(3): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1876741 | |||||
| chr11:1876793 | C | T | 1 | a0002c0001t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.54-3294C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876793 | ||||||
| chr11:1876853 | T | A | 1 | a0002c0001t0001g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.54-3234T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876853 | ||||||
| chr11:1876948 | G | C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-3139G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1876948 | ||||||
| chr11:1877050 | C | T | 1 | a0002c0001t0001g0029 | 2 | NA18954.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.54-3037C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877050 | ||||||
| chr11:1877200 | C | T | 1 | a0002c0005t0001g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.54-2887C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877200 | ||||||
| chr11:1877205 | C | G | 1 | a0003c0004t0001g0283 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.54-2882C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877205 | ||||||
| chr11:1877272 | G | A | 1 | a0007c0015t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-2815G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877272 | ||||||
| chr11:1877292 | T | C | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-2795T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877292 | ||||||
| chr11:1877312 | T | G | 290 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(287): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.54-2775T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877312 | ||||||
| chr11:1877387 | C | T | 2 | a0004c0008t0001g0164a0004c0008t0001g0183 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.54-2700C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877387 | ||||||
| chr11:1877434 | T | C | 134 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(131): Show | 176 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.54-2653T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877434 | ||||||
| chr11:1877534 | C | T | 2 | a0004c0008t0001g0164a0004c0008t0001g0183 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.54-2553C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877534 | ||||||
| chr11:1877543 | A | G | 1 | a0003c0006t0001g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.54-2544A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877543 | ||||||
| chr11:1877638 | A | AG | 48 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(45): Show | 53 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.54-2444dupG | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1877638 | |||||
| chr11:1877679 | G | A | 1 | a0001c0018t0001g0137 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.54-2408G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877679 | ||||||
| chr11:1877844 | C | T | 9 | a0002c0001t0001g0006a0002c0001t0001g0249a0002c0001t0001g0251others(6): Show | 11 | HG00408.hp2 NA18943.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-2243C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877844 | ||||||
| chr11:1877908 | C | T | 1 | a0001c0003t0001g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.54-2179C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877908 | ||||||
| chr11:1877992 | C | A | 1 | a0001c0002t0001g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.54-2095C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877992 | ||||||
| chr11:1877996 | G | C | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-2091G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1877996 | ||||||
| chr11:1878166 | C | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(2): Show | 8 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-1921C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878166 | ||||||
| chr11:1878167 | G | A | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1920G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878167 | ||||||
| chr11:1878234 | TGC | T | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1850_54-1849del others(2): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1878234 | |||||
| chr11:1878235 | G | A | 2 | a0001c0003t0001g0043a0001c0003t0001g0057 | 2 | NA18983.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.54-1852G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878235 | ||||||
| chr11:1878236 | C | T | 1 | a0002c0001t0001g0277 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.54-1851C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878236 | ||||||
| chr11:1878247 | G | A | 1 | a0002c0001t0001g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-1840G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878247 | ||||||
| chr11:1878277 | G | A | 1 | a0001c0002t0001g0023 | 2 | NA18948.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.54-1810G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878277 | ||||||
| chr11:1878288 | C | T | 1 | a0001c0002t0001g0135 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.54-1799C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878288 | ||||||
| chr11:1878342 | C | T | 1 | a0002c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.54-1745C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878342 | ||||||
| chr11:1878351 | G | T | 1 | a0003c0004t0001g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.54-1736G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878351 | ||||||
| chr11:1878382 | G | A | 5 | a0001c0002t0001g0181a0002c0001t0001g0009a0002c0001t0001g0280others(2): Show | 8 | HG00558.hp1 HG00733.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-1705G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878382 | ||||||
| chr11:1878429 | C | G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1658C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878429 | ||||||
| chr11:1878435 | T | A | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-1652T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878435 | ||||||
| chr11:1878473 | TCGGGGGC others(1): Show |
T | 2 | a0002c0001t0002g0016a0002c0001t0002g0041 | 4 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1607_54-1600del others(8): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 1878473 | |||||
| chr11:1878512 | T | G | 1 | a0001c0002t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.54-1575T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878512 | ||||||
| chr11:1878521 | G | A | 1 | a0002c0016t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54-1566G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878521 | ||||||
| chr11:1878545 | G | A | 19 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0017others(16): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.54-1542G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878545 | ||||||
| chr11:1878669 | T | A | 48 | a0001c0003t0001g0258a0002c0001t0001g0215a0002c0001t0001g0216others(45): Show | 53 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.54-1418T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878669 | ||||||
| chr11:1878707 | C | G | 4 | a0003c0004t0001g0195a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1380C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878707 | ||||||
| chr11:1878732 | G | A | 43 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(40): Show | 58 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.54-1355G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878732 | ||||||
| chr11:1878795 | C | T | 19 | a0001c0002t0001g0005a0001c0002t0001g0014a0001c0002t0001g0023others(16): Show | 28 | HG00438.hp1 HG02027.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-1292C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878795 | ||||||
| chr11:1878849 | A | G | 1 | a0002c0001t0001g0276 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.54-1238A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1878849 | ||||||
| chr11:1879023 | T | C | 1 | a0001c0003t0001g0270 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.54-1064T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879023 | ||||||
| chr11:1879059 | A | C | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54-1028A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879059 | ||||||
| chr11:1879062 | C | G | 1 | a0002c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.54-1025C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879062 | ||||||
| chr11:1879119 | C | A | 1 | a0002c0005t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.54-968C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879119 | ||||||
| chr11:1879164 | G | T | 1 | a0001c0002t0001g0127 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.54-923G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879164 | ||||||
| chr11:1879183 | A | G | 1 | a0001c0002t0001g0022 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.54-904A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879183 | ||||||
| chr11:1879211 | G | A | 26 | a0002c0001t0001g0006a0002c0001t0001g0035a0002c0001t0001g0205others(23): Show | 29 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.54-876G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879211 | ||||||
| chr11:1879347 | A | G | 1 | a0003c0004t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.54-740A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879347 | ||||||
| chr11:1879440 | C | A | 6 | a0002c0001t0002g0016a0002c0001t0002g0041a0002c0001t0002g0175others(3): Show | 8 | HG00280.hp2 HG00735.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-647C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879440 | ||||||
| chr11:1879471 | C | T | 45 | a0001c0002t0001g0022a0001c0002t0001g0104a0001c0002t0001g0125others(42): Show | 61 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.54-616C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879471 | ||||||
| chr11:1879526 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.54-561C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879526 | ||||||
| chr11:1879535 | C | T | 56 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(53): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.54-552C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879535 | ||||||
| chr11:1879618 | G | A | 1 | a0003c0004t0003g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.54-469G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879618 | ||||||
| chr11:1879650 | G | A | 3 | a0002c0001t0001g0012a0002c0001t0001g0079a0002c0001t0001g0080 | 5 | HG00544.hp2 NA18964.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-437G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879650 | ||||||
| chr11:1879935 | G | A | 27 | a0002c0001t0001g0006a0002c0001t0001g0035a0002c0001t0001g0189others(24): Show | 32 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.54-152G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879935 | ||||||
| chr11:1879989 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.54-98C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 1/10 | chr11 | 1879989 | ||||||
| chr11:1880237 | A | C | 200 | a0001c0002t0001g0100a0001c0002t0001g0200a0001c0003t0001g0001others(197): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.191+13A>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880237 | ||||||
| chr11:1880241 | C | T | 1 | a0002c0001t0001g0228 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.191+17C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880241 | ||||||
| chr11:1880268 | G | A | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.191+44G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880268 | ||||||
| chr11:1880524 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.191+300C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880524 | ||||||
| chr11:1880617 | C | T | 31 | a0002c0001t0001g0006a0002c0001t0001g0035a0002c0001t0001g0189others(28): Show | 36 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.191+393C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880617 | ||||||
| chr11:1880707 | T | A | 27 | a0002c0001t0001g0006a0002c0001t0001g0035a0002c0001t0001g0189others(24): Show | 30 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.191+483T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880707 | ||||||
| chr11:1880867 | C | T | 67 | a0002c0001t0001g0008a0002c0001t0001g0009a0002c0001t0001g0012others(64): Show | 82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.192-565C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880867 | ||||||
| chr11:1880949 | A | G | 1 | a0003c0006t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.192-483A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1880949 | ||||||
| chr11:1881245 | G | A | 113 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(110): Show | 154 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.192-187G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881245 | ||||||
| chr11:1881255 | T | C | 50 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(47): Show | 72 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.192-177T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881255 | ||||||
| chr11:1881274 | T | C | 1 | a0003c0004t0001g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.192-158T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881274 | ||||||
| chr11:1881405 | G | T | 272 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(269): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.192-27G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881405 | ||||||
| chr11:1881418 | C | G | 1 | a0003c0004t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192-14C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881418 | ||||||
| chr11:1881418 | C | T | 1 | a0001c0003t0001g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.192-14C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 2/10 | chr11 | 1881418 | ||||||
| chr11:1881607 | G | GCCTCGAG others(34): Show |
1 | a0002c0005t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.356+84_356+124dupT others(40): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 1881607 | |||||
| chr11:1881607 | G | GCCTCGAG others(75): Show |
35 | a0002c0001t0001g0071a0002c0001t0001g0083a0002c0001t0001g0169others(32): Show | 35 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.356+43_356+124dupT others(81): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 1881607 | |||||
| chr11:1881607 | GCCTCGAG others(34): Show |
G | 28 | a0001c0003t0001g0185a0002c0001t0001g0006a0002c0001t0001g0035others(25): Show | 31 | HG00408.hp2 HG00733.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.356+84_356+124delT others(40): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 1881607 | |||||
| chr11:1881617 | C | T | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.356+21C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881617 | ||||||
| chr11:1881693 | C | T | 15 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(12): Show | 18 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.356+97C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881693 | ||||||
| chr11:1881723 | C | T | 16 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(13): Show | 19 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.356+127C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881723 | ||||||
| chr11:1881724 | G | A | 27 | a0002c0001t0001g0006a0002c0001t0001g0035a0002c0001t0001g0189others(24): Show | 30 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.356+128G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881724 | ||||||
| chr11:1881753 | G | C | 2 | a0002c0001t0001g0267a0002c0001t0005g0266 | 2 | HG00323.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.356+157G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881753 | ||||||
| chr11:1881818 | G | C | 2 | a0002c0005t0001g0099a0002c0016t0001g0098 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.356+222G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881818 | ||||||
| chr11:1881834 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.356+238G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881834 | ||||||
| chr11:1881953 | T | C | 1 | a0003c0004t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.356+357T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881953 | ||||||
| chr11:1881975 | G | A | 2 | a0003c0004t0001g0226a0003c0004t0001g0229 | 2 | NA18612.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.356+379G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881975 | ||||||
| chr11:1881984 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.356+388C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1881984 | ||||||
| chr11:1882083 | C | T | 1 | a0002c0005t0001g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.356+487C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882083 | ||||||
| chr11:1882091 | C | T | 7 | a0002c0001t0001g0006a0002c0001t0001g0249a0002c0001t0001g0251others(4): Show | 9 | NA18943.hp2 NA18952.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.356+495C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882091 | ||||||
| chr11:1882196 | G | A | 44 | a0003c0004t0001g0031a0003c0004t0001g0032a0003c0004t0001g0033others(41): Show | 49 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.356+600G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882196 | ||||||
| chr11:1882207 | C | T | 1 | a0003c0004t0001g0231 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.356+611C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882207 | ||||||
| chr11:1882657 | G | A | 1 | a0001c0003t0001g0044 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.357-762G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882657 | ||||||
| chr11:1882870 | C | T | 1 | a0002c0001t0001g0035 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.357-549C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882870 | ||||||
| chr11:1882964 | C | A | 2 | a0002c0001t0001g0205a0002c0001t0001g0252 | 2 | NA18944.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.357-455C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1882964 | ||||||
| chr11:1883048 | C | T | 1 | a0002c0016t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.357-371C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883048 | ||||||
| chr11:1883169 | C | T | 27 | a0002c0001t0001g0029a0002c0001t0001g0160a0002c0001t0001g0165others(24): Show | 32 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.357-250C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883169 | ||||||
| chr11:1883170 | C | T | 27 | a0002c0001t0001g0029a0002c0001t0001g0160a0002c0001t0001g0165others(24): Show | 32 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.357-249C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883170 | ||||||
| chr11:1883201 | G | A | 42 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.357-218G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883201 | ||||||
| chr11:1883298 | C | T | 10 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(7): Show | 13 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.357-121C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883298 | ||||||
| chr11:1883355 | A | T | 1 | a0002c0001t0001g0259 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.357-64A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883355 | ||||||
| chr11:1883392 | C | T | 1 | a0001c0003t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.357-27C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 3/10 | chr11 | 1883392 | ||||||
| chr11:1883617 | C | T | 1 | a0001c0003t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.498+57C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | chr11 | 1883617 | ||||||
| chr11:1883687 | G | A | 1 | a0003c0006t0001g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.498+127G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | chr11 | 1883687 | ||||||
| chr11:1883688 | A | G | 1 | a0002c0005t0001g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498+128A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | chr11 | 1883688 | ||||||
| chr11:1883758 | A | T | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.499-174A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | chr11 | 1883758 | ||||||
| chr11:1883759 | G | C | 46 | a0001c0002t0001g0113a0001c0002t0001g0144a0001c0003t0001g0001others(43): Show | 63 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.499-173G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | chr11 | 1883759 | ||||||
| chr11:1883916 | G | GT | 25 | a0001c0002t0001g0005a0001c0002t0001g0014a0001c0002t0001g0023others(22): Show | 34 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.499-5dupT | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 1883916 | |||||
| chr11:1883916 | GT | G | 29 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(26): Show | 29 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.499-5delT | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 1883916 | |||||
| chr11:1884062 | T | C | 114 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(111): Show | 158 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.591+38T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 5/10 | chr11 | 1884062 | ||||||
| chr11:1884423 | G | C | 25 | a0002c0001t0001g0029a0002c0001t0001g0077a0002c0001t0001g0078others(22): Show | 30 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.636-77G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 6/10 | chr11 | 1884423 | ||||||
| chr11:1884851 | A | G | 1 | a0002c0001t0001g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.717+270A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1884851 | ||||||
| chr11:1884937 | C | T | 1 | a0002c0005t0001g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.717+356C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1884937 | ||||||
| chr11:1884938 | G | A | 1 | a0001c0003t0001g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+357G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1884938 | ||||||
| chr11:1884944 | G | A | 154 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(151): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.717+363G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1884944 | ||||||
| chr11:1885061 | C | G | 55 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(52): Show | 61 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.717+480C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885061 | ||||||
| chr11:1885152 | T | C | 1 | a0001c0003t0001g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+571T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885152 | ||||||
| chr11:1885316 | A | G | 1 | a0002c0001t0001g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.717+735A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885316 | ||||||
| chr11:1885472 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.717+891A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885472 | ||||||
| chr11:1885585 | C | A | 55 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(52): Show | 61 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.717+1004C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885585 | ||||||
| chr11:1885669 | T | A | 3 | a0001c0002t0001g0132a0002c0001t0001g0246a0002c0001t0001g0259 | 3 | NA18973.hp2 NA18979.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.718-1063T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885669 | ||||||
| chr11:1885812 | C | T | 1 | a0002c0001t0001g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-920C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885812 | ||||||
| chr11:1885887 | C | T | 45 | a0001c0002t0001g0132a0002c0001t0001g0006a0002c0001t0001g0029others(42): Show | 53 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-845C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885887 | ||||||
| chr11:1885902 | A | G | 1 | a0002c0005t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-830A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885902 | ||||||
| chr11:1885903 | T | C | 154 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(151): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.718-829T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1885903 | ||||||
| chr11:1886071 | C | T | 6 | a0002c0005t0001g0013a0002c0005t0001g0097a0002c0005t0001g0118others(3): Show | 7 | HG00558.hp2 HG02027.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-661C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886071 | ||||||
| chr11:1886191 | C | T | 56 | a0001c0002t0001g0200a0001c0003t0001g0168a0001c0003t0001g0170others(53): Show | 60 | HG00323.hp2 HG00408.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.718-541C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886191 | ||||||
| chr11:1886192 | G | A | 45 | a0001c0002t0001g0132a0002c0001t0001g0006a0002c0001t0001g0029others(42): Show | 53 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-540G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886192 | ||||||
| chr11:1886311 | A | G | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-421A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886311 | ||||||
| chr11:1886379 | C | G | 99 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(96): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.718-353C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886379 | ||||||
| chr11:1886380 | T | C | 56 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(53): Show | 62 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.718-352T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886380 | ||||||
| chr11:1886423 | T | C | 270 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(267): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.718-309T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886423 | ||||||
| chr11:1886457 | C | T | 154 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(151): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.718-275C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886457 | ||||||
| chr11:1886471 | C | G | 1 | a0002c0001t0001g0214 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.718-261C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886471 | ||||||
| chr11:1886550 | C | G | 2 | a0003c0004t0001g0241a0003c0004t0001g0242 | 2 | HG00642.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.718-182C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886550 | ||||||
| chr11:1886690 | G | A | 1 | a0002c0001t0001g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.718-42G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886690 | ||||||
| chr11:1886710 | T | C | 154 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(151): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.718-22T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 7/10 | chr11 | 1886710 | ||||||
| chr11:1887051 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.852+185G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 8/10 | chr11 | 1887051 | ||||||
| chr11:1887136 | C | T | 1 | a0002c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.853-101C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 8/10 | chr11 | 1887136 | ||||||
| chr11:1887397 | G | T | 1 | a0002c0011t0010g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.931-77G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 9/10 | chr11 | 1887397 | ||||||
| chr11:1887671 | C | T | 9 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(6): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.*13+95C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887671 | ||||||
| chr11:1887725 | C | T | 1 | a0001c0003t0001g0054 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.*13+149C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887725 | ||||||
| chr11:1887767 | C | A | 2 | a0003c0004t0001g0241a0003c0004t0001g0242 | 2 | HG00642.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.*13+191C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887767 | ||||||
| chr11:1887776 | T | C | 59 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(56): Show | 66 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.*13+200T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887776 | ||||||
| chr11:1887851 | C | T | 1 | a0003c0006t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*13+275C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887851 | ||||||
| chr11:1887974 | T | C | 1 | a0001c0002t0001g0005 | 5 | NA18945.hp1 NA18946.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*13+398T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887974 | ||||||
| chr11:1887980 | G | A | 1 | a0001c0003t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.*13+404G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887980 | ||||||
| chr11:1887994 | T | C | 2 | a0001c0002t0001g0110a0002c0001t0001g0076 | 2 | HG00438.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.*13+418T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887994 | ||||||
| chr11:1887998 | A | T | 1 | a0001c0003t0001g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.*13+422A>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1887998 | ||||||
| chr11:1888386 | C | A | 18 | a0001c0018t0001g0137a0003c0004t0001g0033a0003c0004t0001g0060others(15): Show | 19 | HG00408.hp1 HG02071.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.*13+810C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888386 | ||||||
| chr11:1888441 | G | A | 2 | a0003c0004t0001g0208a0003c0004t0001g0210 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.*13+865G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888441 | ||||||
| chr11:1888493 | AGGT | A | 11 | a0002c0005t0001g0015a0002c0005t0001g0027a0002c0005t0001g0148others(8): Show | 14 | HG00639.hp1 HG00642.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.*13+920_*13+922del others(3): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 1888493 | |||||
| chr11:1888558 | C | T | 12 | a0001c0003t0001g0168a0001c0003t0001g0170a0001c0003t0001g0198others(9): Show | 12 | HG02451.hp2 HG02602.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.*13+982C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888558 | ||||||
| chr11:1888704 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*13+1128C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888704 | ||||||
| chr11:1888885 | G | A | 2 | a0002c0001t0004g0030a0002c0001t0004g0190 | 3 | HG01243.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.*13+1309G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888885 | ||||||
| chr11:1888989 | T | A | 3 | a0002c0001t0001g0161a0002c0001t0001g0162a0002c0001t0001g0163 | 3 | HG01433.hp2 HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*13+1413T>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888989 | ||||||
| chr11:1888996 | C | T | 1 | a0003c0004t0001g0227 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*13+1420C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1888996 | ||||||
| chr11:1889034 | C | T | 1 | a0003c0004t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*13+1458C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889034 | ||||||
| chr11:1889072 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.*13+1496C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889072 | ||||||
| chr11:1889234 | G | A | 1 | a0003c0004t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*13+1658G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889234 | ||||||
| chr11:1889338 | C | A | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.*13+1762C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889338 | ||||||
| chr11:1889355 | C | T | 1 | a0002c0005t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*13+1779C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889355 | ||||||
| chr11:1889398 | C | T | 1 | a0001c0003t0001g0019 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*13+1822C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889398 | ||||||
| chr11:1889405 | C | T | 13 | a0002c0001t0001g0077a0002c0001t0001g0078a0002c0001t0001g0160others(10): Show | 14 | HG00099.hp2 HG01106.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.*13+1829C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889405 | ||||||
| chr11:1889453 | CAGGCACC others(17): Show |
C | 1 | a0003c0006t0001g0234 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.*13+1878_*13+1901d others(26): Show |
LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889453 | ||||||
| chr11:1889477 | T | C | 280 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(277): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.*13+1901T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889477 | ||||||
| chr11:1889477 | T | G | 1 | a0001c0002t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*13+1901T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889477 | ||||||
| chr11:1889482 | A | G | 9 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(6): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.*13+1906A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889482 | ||||||
| chr11:1889517 | C | T | 2 | a0001c0002t0001g0107a0003c0004t0001g0031 | 3 | HG01358.hp2 NA18982.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.*13+1941C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889517 | ||||||
| chr11:1889624 | G | A | 6 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(3): Show | 9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.*13+2048G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889624 | ||||||
| chr11:1889885 | T | C | 269 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(266): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.*14-1888T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889885 | ||||||
| chr11:1889934 | G | T | 1 | a0001c0002t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*14-1839G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1889934 | ||||||
| chr11:1890055 | T | G | 1 | a0001c0003t0001g0065 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.*14-1718T>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890055 | ||||||
| chr11:1890065 | C | G | 1 | a0003c0004t0001g0204 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*14-1708C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890065 | ||||||
| chr11:1890094 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*14-1679G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890094 | ||||||
| chr11:1890101 | G | A | 1 | a0003c0006t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.*14-1672G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890101 | ||||||
| chr11:1890110 | C | T | 9 | a0001c0003t0001g0007a0001c0003t0001g0037a0001c0003t0001g0038others(6): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.*14-1663C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890110 | ||||||
| chr11:1890141 | G | T | 1 | a0001c0003t0001g0065 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.*14-1632G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890141 | ||||||
| chr11:1890209 | G | T | 44 | a0001c0003t0001g0168a0001c0003t0001g0170a0001c0003t0001g0198others(41): Show | 48 | HG00408.hp1 HG00642.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.*14-1564G>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890209 | ||||||
| chr11:1890227 | T | C | 4 | a0002c0005t0003g0155a0003c0004t0003g0187a0003c0004t0003g0196others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.*14-1546T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890227 | ||||||
| chr11:1890324 | C | T | 2 | a0002c0005t0001g0126a0002c0005t0009g0085 | 2 | HG03486.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.*14-1449C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890324 | ||||||
| chr11:1890446 | G | C | 1 | a0002c0001t0001g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*14-1327G>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890446 | ||||||
| chr11:1890555 | G | A | 1 | a0002c0005t0001g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*14-1218G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890555 | ||||||
| chr11:1890581 | G | A | 1 | a0002c0001t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.*14-1192G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890581 | ||||||
| chr11:1890603 | G | A | 1 | a0003c0004t0001g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.*14-1170G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890603 | ||||||
| chr11:1890660 | T | C | 282 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(279): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.*14-1113T>C | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890660 | ||||||
| chr11:1890661 | G | A | 2 | a0001c0003t0001g0019a0003c0006t0001g0103 | 3 | HG01256.hp1 HG01258.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.*14-1112G>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890661 | ||||||
| chr11:1890907 | C | A | 1 | a0001c0003t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*14-866C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1890907 | ||||||
| chr11:1891066 | A | G | 148 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(145): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.*14-707A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891066 | ||||||
| chr11:1891128 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*14-645C>A | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891128 | ||||||
| chr11:1891129 | C | T | 1 | a0002c0001t0001g0255 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.*14-644C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891129 | ||||||
| chr11:1891205 | C | G | 1 | a0001c0003t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*14-568C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891205 | ||||||
| chr11:1891300 | C | G | 1 | a0002c0005t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.*14-473C>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891300 | ||||||
| chr11:1891496 | A | G | 145 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(142): Show | 194 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.*14-277A>G | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891496 | ||||||
| chr11:1891520 | C | T | 33 | a0001c0002t0001g0104a0001c0002t0001g0125a0001c0002t0001g0138others(30): Show | 34 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.*14-253C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891520 | ||||||
| chr11:1891732 | C | T | 3 | a0002c0001t0004g0030a0002c0001t0004g0190a0002c0005t0009g0085 | 4 | HG01243.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.*14-41C>T | LSP1 | ENSG00000130592.17 | transcript | ENST00000311604.8 | protein_coding | 10/10 | chr11 | 1891732 |