Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 91624 |
|---|---|
| ensemblid | ENSG00000162614.19 |
| hgncid | 29557 |
| symbol | NEXN |
| name | nexilin F-actin binding protein |
| refseq_nuc | NM_144573.4 |
| refseq_prot | NP_653174.3 |
| ensembl_nuc | ENST00000334785.12 |
| ensembl_prot | ENSP00000333938.7 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 77888624 |
| end | 77943895 |
| strand | + |
| ver | v1.2 |
| region | chr1:77888624-77943895 |
| region5000 | chr1:77883624-77948895 |
| regionname0 | NEXN_chr1_77888624_77943895 |
| regionname5000 | NEXN_chr1_77883624_77948895 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 675 | 231 | 73 | 50 | 65 | 8 | 33 | 45 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0002 | 0/0 | 675 | 33 | 0 | 9 | 19 | 4 | 1 | 14 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0003 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0004 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0005 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0006 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2028 | 223 | 65 | 50 | 65 | 8 | 33 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0002 | 0/0 | 2028 | 33 | 0 | 9 | 19 | 4 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0003 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0004 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0005 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0006 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0007 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0008 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| c0009 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1255 | 160 | 42 | 46 | 38 | 10 | 22 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0002 | 0/0 | 1255 | 38 | 2 | 9 | 21 | 2 | 4 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0003 | 0/0 | 1248 | 28 | 8 | 0 | 19 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0004 | 0/0 | 1256 | 16 | 4 | 2 | 3 | 0 | 7 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0005 | 0/0 | 1256 | 5 | 5 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0006 | 0/0 | 1255 | 4 | 3 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0007 | 0/0 | 1256 | 4 | 4 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0008 | 0/0 | 1248 | 3 | 0 | 0 | 3 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0009 | 0/0 | 1256 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0010 | 0/0 | 1256 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0011 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0012 | 0/0 | 1255 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0013 | 0/0 | 1255 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0014 | 0/0 | 1255 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0015 | 0/0 | 1255 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0016 | 0/0 | 1255 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| t0017 | 0/0 | 1256 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2028 | 223 | 65 | 50 | 65 | 8 | 33 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0003 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0008 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0009 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0002c0002 | 0/0 | 2028 | 33 | 0 | 9 | 19 | 4 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0003c0007 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0004c0006 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0005c0005 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0006c0004 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3282 | 123 | 40 | 37 | 17 | 6 | 21 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0002 | 0/0 | 3282 | 37 | 2 | 8 | 21 | 2 | 4 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0003 | 0/0 | 3275 | 28 | 8 | 0 | 19 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0004 | 0/0 | 3283 | 12 | 0 | 2 | 3 | 0 | 7 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0005 | 0/0 | 3283 | 5 | 5 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0006 | 0/0 | 3282 | 4 | 3 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0007 | 0/0 | 3283 | 4 | 4 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0008 | 0/0 | 3275 | 3 | 0 | 0 | 3 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0010 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0011 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0013 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0014 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0015 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0016 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0001t0017 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0003t0004 | 0/0 | 3283 | 4 | 4 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0003t0009 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0008t0001 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0001c0009t0012 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0002c0002t0001 | 0/0 | 3282 | 33 | 0 | 9 | 19 | 4 | 1 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0003c0007t0002 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0004c0006t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0005c0005t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| a0006c0004t0001 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | copy fasta | chr1 | 77883624 | 77948895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0014g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0016g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0017g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0008t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0009t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0003c0007t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0004c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0005c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0006c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0259 | EUR | GBR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0049 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0009 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01346 | hp2 | a0003 | c0007 | t0002 | g0196 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0059 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0241 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0176 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0117 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02040 | hp2 | a0005 | c0005 | t0001 | g0082 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0102 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02145 | hp2 | a0001 | c0009 | t0012 | g0165 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CDX | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02258 | hp1 | a0001 | c0001 | t0014 | g0204 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0168 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0151 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02615 | hp2 | a0001 | c0008 | t0001 | g0068 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02818 | hp2 | a0001 | c0003 | t0009 | g0162 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0161 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03130 | hp2 | a0006 | c0004 | t0001 | g0064 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0163 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0159 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0134 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | CHB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0211 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18969 | hp1 | a0004 | c0006 | t0001 | g0222 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | LWK | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19065 | hp2 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ASW | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0242 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | GIH | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | GIH | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0164 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20300 | hp2 | a0001 | c0003 | t0004 | g0203 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0123 | REF | REF | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0147 | REF | REF | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77917990
|
G | A | 1 | a0006 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.250G>A | p.Glu84Lys | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 4/13 | 438/3282 | 250/2028 | 84/675 | chr1 | 77917990 | ||
| chr1:77926436
|
T | C | 1 | a0005 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.512T>C | p.Ile171Thr | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 7/13 | 700/3282 | 512/2028 | 171/675 | chr1 | 77926436 | ||
| chr1:77926761
|
G | A | 2 | a0002a0004 | 34 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
missense_variant | MODERATE | c.733G>A | p.Gly245Arg | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/13 | 921/3282 | 733/2028 | 245/675 | chr1 | 77926761 | ||
| chr1:77936006
|
C | T | 1 | a0003 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1435C>T | p.Leu479Phe | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/13 | 1623/3282 | 1435/2028 | 479/675 | chr1 | 77936006 | ||
| chr1:77942623
|
G | A | 1 | a0004 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1822G>A | p.Glu608Lys | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 2010/3282 | 1822/2028 | 608/675 | chr1 | 77942623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77917694
|
C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.156C>T | p.Asp52Asp | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 3/13 | 344/3282 | 156/2028 | 52/675 | chr1 | 77917694 | ||
| chr1:77918189
|
G | A | 1 | a0001c0003 | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
synonymous_variant | LOW | c.363G>A | p.Thr121Thr | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/13 | 551/3282 | 363/2028 | 121/675 | chr1 | 77918189 | ||
| chr1:77926805
|
A | G | 2 | a0001c0008a0006c0004 | 2 | HG02615.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.777A>G | p.Gln259Gln | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/13 | 965/3282 | 777/2028 | 259/675 | chr1 | 77926805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77888661
|
G | A | 1 | a0001c0001t0010 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/13 | 27446 | chr1 | 77888661 | |||||
| chr1:77942851
|
C | G | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(3): Show | 46 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 22 | chr1 | 77942851 | |||||
| chr1:77943108
|
G | A | 1 | a0001c0001t0006 | 4 | HG01109.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*279G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 279 | chr1 | 77943108 | |||||
| chr1:77943143
|
A | C | 1 | a0001c0003t0009 | 2 | HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*314A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 314 | chr1 | 77943143 | |||||
| chr1:77943237
|
C | CA | 4 | a0001c0001t0004a0001c0001t0011a0001c0003t0004others(1): Show | 19 | HG01255.hp2 HG01496.hp2 HG02056.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*418dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 419 | INFO_REALIGN_3_PRIME | chr1 | 77943237 | ||||
| chr1:77943246
|
A | AC | 3 | a0001c0001t0005a0001c0001t0010a0001c0001t0017 | 7 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*418insC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 418 | chr1 | 77943246 | |||||
| chr1:77943289
|
T | A | 1 | a0001c0009t0012 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*460T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 460 | chr1 | 77943289 | |||||
| chr1:77943338
|
T | TA | 1 | a0001c0001t0007 | 4 | HG02897.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*511dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 512 | INFO_REALIGN_3_PRIME | chr1 | 77943338 | ||||
| chr1:77943345
|
T | C | 1 | a0001c0001t0013 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 516 | chr1 | 77943345 | |||||
| chr1:77943482
|
A | G | 1 | a0001c0001t0015 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 653 | chr1 | 77943482 | |||||
| chr1:77943524
|
G | A | 1 | a0001c0001t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*695G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 695 | chr1 | 77943524 | |||||
| chr1:77943535
|
CAGTGTTG | C | 3 | a0001c0001t0003a0001c0001t0008a0001c0001t0011 | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*722delTGTTGA others(1): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 716 | INFO_REALIGN_3_PRIME | chr1 | 77943535 | ||||
| chr1:77943588
|
T | A | 1 | a0001c0003t0009 | 2 | HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*759T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 759 | chr1 | 77943588 | |||||
| chr1:77943674
|
C | T | 1 | a0001c0001t0017 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 845 | chr1 | 77943674 | |||||
| chr1:77943846
|
A | G | 1 | a0001c0001t0008 | 3 | NA18946.hp2 NA19060.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 1017 | chr1 | 77943846 | |||||
| chr1:77943849
|
T | A | 1 | a0001c0001t0016 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1020T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 1020 | chr1 | 77943849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77888790
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-53+31G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888790 | ||||||
| chr1:77888795
|
T | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG01255.hp1 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+36T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888795 | ||||||
| chr1:77888843
|
C | A | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+84C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888843 | ||||||
| chr1:77888900
|
G | T | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(61): Show | 65 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-53+141G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888900 | ||||||
| chr1:77888907
|
G | C | 1 | a0001c0001t0003g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+148G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888907 | ||||||
| chr1:77888908
|
C | G | 1 | a0001c0001t0003g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+149C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888908 | ||||||
| chr1:77888987
|
C | G | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+228C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888987 | ||||||
| chr1:77888988
|
G | C | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+229G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888988 | ||||||
| chr1:77889117
|
A | T | 1 | a0001c0003t0004g0203 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-53+358A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889117 | ||||||
| chr1:77889310
|
T | TC | 47 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0193others(44): Show | 48 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+559dupC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77889310 | |||||
| chr1:77889319
|
A | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-53+560A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889319 | ||||||
| chr1:77889353
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+594C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889353 | ||||||
| chr1:77889355
|
CT | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-53+612delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77889355 | |||||
| chr1:77889356
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+597T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889356 | ||||||
| chr1:77889756
|
A | T | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+997A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889756 | ||||||
| chr1:77890034
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-53+1275C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890034 | ||||||
| chr1:77890097
|
G | A | 1 | a0001c0001t0017g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-53+1338G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890097 | ||||||
| chr1:77890117
|
A | G | 3 | a0001c0001t0002g0157a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG00609.hp1 NA19078.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-53+1358A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890117 | ||||||
| chr1:77890180
|
A | T | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1421A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890180 | ||||||
| chr1:77890679
|
AGCGGCCT others(5): Show |
A | 1 | a0001c0001t0001g0018 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-53+1922_-53+1933d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77890679 | |||||
| chr1:77890716
|
A | T | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1957A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890716 | ||||||
| chr1:77890717
|
T | A | 1 | a0001c0001t0002g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1958T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890717 | ||||||
| chr1:77890727
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-53+1968C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890727 | ||||||
| chr1:77890871
|
G | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-53+2112G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890871 | ||||||
| chr1:77890999
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.-53+2240C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890999 | ||||||
| chr1:77891747
|
T | TA | 12 | a0001c0001t0002g0015a0001c0001t0002g0148a0001c0001t0002g0149others(9): Show | 12 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.-53+3011dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | |||||
| chr1:77891747
|
TA | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG00639.hp1 HG00735.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.-53+3011delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | |||||
| chr1:77891747
|
TAA | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0022others(6): Show | 9 | HG00438.hp1 HG01175.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53+3010_-53+3011d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | |||||
| chr1:77891747
|
TAAA | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(191): Show |
intron_variant | MODIFIER | c.-53+3009_-53+3011d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | |||||
| chr1:77892061
|
C | T | 1 | a0002c0002t0001g0259 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-53+3302C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892061 | ||||||
| chr1:77892062
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-53+3303A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892062 | ||||||
| chr1:77892082
|
C | CA | 26 | a0001c0001t0002g0157a0001c0001t0002g0178a0001c0001t0002g0234others(23): Show | 27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-53+3335dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77892082 | |||||
| chr1:77892244
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-53+3485C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892244 | ||||||
| chr1:77892411
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-53+3652C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892411 | ||||||
| chr1:77892583
|
T | C | 6 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53+3824T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892583 | ||||||
| chr1:77892607
|
A | G | 1 | a0003c0007t0002g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-53+3848A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892607 | ||||||
| chr1:77892778
|
A | G | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+4019A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892778 | ||||||
| chr1:77892793
|
T | C | 1 | a0001c0003t0004g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-53+4034T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892793 | ||||||
| chr1:77892884
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-53+4125T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892884 | ||||||
| chr1:77893141
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+4382A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893141 | ||||||
| chr1:77893344
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-53+4585T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893344 | ||||||
| chr1:77893434
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-53+4675G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893434 | ||||||
| chr1:77893526
|
C | T | 2 | a0001c0001t0002g0234a0002c0002t0001g0233 | 2 | NA18947.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-53+4767C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893526 | ||||||
| chr1:77893977
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-53+5218G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893977 | ||||||
| chr1:77894273
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-53+5514C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894273 | ||||||
| chr1:77894581
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-53+5822C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894581 | ||||||
| chr1:77894935
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-53+6176C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894935 | ||||||
| chr1:77895029
|
A | AT | 35 | a0001c0001t0001g0028a0001c0001t0001g0133a0001c0001t0001g0193others(32): Show | 36 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-53+6303dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0010g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53+6291_-53+6303d others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0017g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-53+6286_-53+6303d others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
AT | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 61 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-53+6303delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATT | A | 29 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0076others(26): Show | 31 | HG00099.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-53+6302_-53+6303d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTT | A | 16 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0065others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53+6301_-53+6303d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTT | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG02280.hp1 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53+6300_-53+6303d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0002g0194others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6293_-53+6303d others(13): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(5): Show |
A | 8 | a0001c0001t0001g0030a0001c0003t0004g0159a0001c0003t0004g0161others(5): Show | 8 | HG02145.hp2 HG02818.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53+6292_-53+6303d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0001g0023a0001c0001t0001g0062a0001c0001t0001g0160others(1): Show | 4 | HG01261.hp2 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6291_-53+6303d others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(7): Show |
A | 27 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 28 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-53+6290_-53+6303d others(16): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-53+6287_-53+6303d others(19): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895029
|
ATTTTTTT others(11): Show |
A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6286_-53+6303d others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | |||||
| chr1:77895125
|
A | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+6366A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895125 | ||||||
| chr1:77895155
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-53+6396C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895155 | ||||||
| chr1:77895543
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-53+6784A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895543 | ||||||
| chr1:77895721
|
C | T | 2 | a0001c0001t0005g0019a0001c0001t0005g0150 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53+6962C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895721 | ||||||
| chr1:77896170
|
C | CAATAAAT others(1): Show |
25 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 26 | HG00438.hp1 HG02165.hp2 HG02622.hp2 others(23): Show |
intron_variant | MODIFIER | c.-53+7433_-53+7440d others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | |||||
| chr1:77896170
|
C | CAATAAAT others(5): Show |
90 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0020others(87): Show | 93 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-53+7429_-53+7440d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | |||||
| chr1:77896170
|
C | CAATAAAT others(9): Show |
52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(49): Show | 54 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-53+7425_-53+7440d others(18): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | |||||
| chr1:77896170
|
C | CAATAAAT others(13): Show |
18 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(15): Show | 18 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-53+7421_-53+7440d others(22): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | |||||
| chr1:77896170
|
C | CAATAAAT others(17): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0160others(2): Show | 5 | HG00621.hp1 HG00621.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53+7417_-53+7440d others(26): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | |||||
| chr1:77896712
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02976.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-53+7953T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896712 | ||||||
| chr1:77896761
|
T | TA | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | HG03130.hp1 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53+8015dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896761 | |||||
| chr1:77896787
|
A | G | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG00735.hp2 HG02735.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+8028A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896787 | ||||||
| chr1:77896987
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-53+8228A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896987 | ||||||
| chr1:77897099
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+8340A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897099 | ||||||
| chr1:77897162
|
G | A | 7 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(4): Show | 7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+8403G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897162 | ||||||
| chr1:77897340
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53+8581T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897340 | ||||||
| chr1:77897341
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53+8582G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897341 | ||||||
| chr1:77897661
|
G | C | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+8902G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897661 | ||||||
| chr1:77897764
|
C | T | 7 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(4): Show | 7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+9005C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897764 | ||||||
| chr1:77898075
|
GCCATACT others(32): Show |
G | 1 | a0001c0001t0001g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-53+9321_-53+9359d others(41): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77898075 | |||||
| chr1:77898123
|
C | T | 1 | a0001c0001t0005g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-53+9364C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898123 | ||||||
| chr1:77898126
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-53+9367C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898126 | ||||||
| chr1:77898142
|
C | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-53+9383C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898142 | ||||||
| chr1:77898184
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-53+9425A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898184 | ||||||
| chr1:77898760
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0025others(24): Show | 28 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-53+10001C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898760 | ||||||
| chr1:77898875
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0237 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-53+10116G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898875 | ||||||
| chr1:77898914
|
T | A | 1 | a0001c0001t0004g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-53+10155T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898914 | ||||||
| chr1:77898938
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-53+10179A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898938 | ||||||
| chr1:77899025
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-53+10266G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899025 | ||||||
| chr1:77899157
|
G | T | 1 | a0001c0001t0002g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-53+10398G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899157 | ||||||
| chr1:77899272
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-53+10513T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899272 | ||||||
| chr1:77899273
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-53+10514G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899273 | ||||||
| chr1:77899450
|
T | A | 1 | a0001c0001t0002g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-53+10691T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899450 | ||||||
| chr1:77900080
|
T | G | 1 | a0002c0002t0001g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-53+11321T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900080 | ||||||
| chr1:77900163
|
C | T | 2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-53+11404C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900163 | ||||||
| chr1:77900251
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-53+11492T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900251 | ||||||
| chr1:77900378
|
A | G | 1 | a0001c0003t0004g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-53+11619A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900378 | ||||||
| chr1:77900660
|
T | G | 3 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0211 | 3 | HG02922.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+11901T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900660 | ||||||
| chr1:77901027
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-53+12268A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901027 | ||||||
| chr1:77901209
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-53+12450A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901209 | ||||||
| chr1:77901474
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-53+12715C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901474 | ||||||
| chr1:77901654
|
A | G | 1 | a0001c0001t0003g0027 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-53+12895A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901654 | ||||||
| chr1:77902119
|
T | A | 4 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0002t0001g0217others(1): Show | 4 | HG01934.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+13360T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902119 | ||||||
| chr1:77902463
|
T | TA | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52-13591dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77902463 | |||||
| chr1:77902556
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-52-13499T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902556 | ||||||
| chr1:77902707
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52-13348T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902707 | ||||||
| chr1:77902973
|
G | T | 1 | a0002c0002t0001g0226 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52-13082G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902973 | ||||||
| chr1:77903100
|
A | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-12955A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903100 | ||||||
| chr1:77903480
|
G | A | 3 | a0002c0002t0001g0220a0002c0002t0001g0229a0004c0006t0001g0222 | 3 | NA18969.hp1 NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-52-12575G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903480 | ||||||
| chr1:77903527
|
T | G | 55 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 58 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(55): Show |
intron_variant | MODIFIER | c.-52-12528T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903527 | ||||||
| chr1:77903761
|
C | CA | 20 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-12288dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77903761 | |||||
| chr1:77903819
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0014g0204 | 3 | HG02258.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-52-12236G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903819 | ||||||
| chr1:77903858
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-52-12197G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903858 | ||||||
| chr1:77903991
|
GTTTTTA | G | 20 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-12052_-52-1204 others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77903991 | |||||
| chr1:77904071
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-52-11984C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904071 | ||||||
| chr1:77904235
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-52-11820C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904235 | ||||||
| chr1:77904449
|
G | A | 20 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-11606G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904449 | ||||||
| chr1:77904486
|
A | G | 1 | a0001c0001t0017g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-52-11569A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904486 | ||||||
| chr1:77904554
|
T | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-11501T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904554 | ||||||
| chr1:77904558
|
G | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52-11497G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904558 | ||||||
| chr1:77904766
|
A | G | 1 | a0001c0009t0012g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-52-11289A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904766 | ||||||
| chr1:77905057
|
A | C | 6 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0016others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-10998A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905057 | ||||||
| chr1:77905133
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-52-10922G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905133 | ||||||
| chr1:77905159
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-52-10896T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905159 | ||||||
| chr1:77905258
|
C | CA | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-52-10786dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77905258 | |||||
| chr1:77905303
|
T | A | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-52-10752T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905303 | ||||||
| chr1:77905306
|
C | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-10749C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905306 | ||||||
| chr1:77905352
|
A | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-10703A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905352 | ||||||
| chr1:77905666
|
A | T | 1 | a0001c0001t0011g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-52-10389A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905666 | ||||||
| chr1:77905706
|
A | G | 7 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(4): Show | 7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52-10349A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905706 | ||||||
| chr1:77905909
|
G | C | 2 | a0001c0003t0004g0159a0001c0003t0004g0161 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-52-10146G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905909 | ||||||
| chr1:77906048
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-10007G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906048 | ||||||
| chr1:77906108
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52-9947G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906108 | ||||||
| chr1:77906188
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-52-9867G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906188 | ||||||
| chr1:77906592
|
T | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-9463T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906592 | ||||||
| chr1:77906767
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-52-9288G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906767 | ||||||
| chr1:77907032
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-52-9023A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907032 | ||||||
| chr1:77907036
|
G | C | 1 | a0001c0001t0006g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-52-9019G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907036 | ||||||
| chr1:77907369
|
G | A | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-8686G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907369 | ||||||
| chr1:77907372
|
G | A | 2 | a0001c0001t0004g0253a0001c0001t0004g0255 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-52-8683G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907372 | ||||||
| chr1:77907604
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-52-8451C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907604 | ||||||
| chr1:77907608
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-52-8447G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907608 | ||||||
| chr1:77908008
|
G | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-8047G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908008 | ||||||
| chr1:77908057
|
T | G | 2 | a0001c0008t0001g0068a0006c0004t0001g0064 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-7998T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908057 | ||||||
| chr1:77908065
|
A | C | 3 | a0002c0002t0001g0242a0002c0002t0001g0243a0002c0002t0001g0251 | 3 | HG00642.hp2 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-52-7990A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908065 | ||||||
| chr1:77908100
|
C | T | 1 | a0001c0003t0004g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-7955C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908100 | ||||||
| chr1:77908181
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0004g0134 | 2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-52-7874G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908181 | ||||||
| chr1:77908231
|
T | C | 123 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(120): Show | 127 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.-52-7824T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908231 | ||||||
| chr1:77908312
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-52-7743C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908312 | ||||||
| chr1:77908370
|
C | T | 2 | a0001c0001t0003g0063a0001c0001t0003g0073 | 2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-52-7685C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908370 | ||||||
| chr1:77908394
|
A | AT | 16 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0058others(13): Show | 17 | HG01099.hp1 HG01255.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-52-7638dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | |||||
| chr1:77908394
|
A | ATT | 5 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 5 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-7639_-52-7638d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | |||||
| chr1:77908394
|
AT | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0026others(36): Show | 41 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-52-7638delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | |||||
| chr1:77908394
|
ATT | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-7639_-52-7638d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | |||||
| chr1:77908493
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-52-7562C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908493 | ||||||
| chr1:77908513
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52-7542G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908513 | ||||||
| chr1:77908620
|
G | A | 2 | a0001c0001t0005g0019a0001c0001t0005g0150 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-52-7435G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908620 | ||||||
| chr1:77908716
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-52-7339A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908716 | ||||||
| chr1:77908861
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-52-7194T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908861 | ||||||
| chr1:77909335
|
G | T | 3 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0192 | 3 | NA18972.hp2 NA18980.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-52-6720G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909335 | ||||||
| chr1:77909440
|
A | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0237a0001c0001t0001g0250others(10): Show | 13 | HG00621.hp2 HG00735.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52-6615A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909440 | ||||||
| chr1:77909674
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-52-6381A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909674 | ||||||
| chr1:77909965
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-52-6090T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909965 | ||||||
| chr1:77910116
|
G | C | 1 | a0001c0003t0004g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-52-5939G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910116 | ||||||
| chr1:77910238
|
CTG | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-5816_-52-5815d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910238 | ||||||
| chr1:77910419
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-52-5636T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910419 | ||||||
| chr1:77910615
|
G | A | 1 | a0002c0002t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-52-5440G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910615 | ||||||
| chr1:77910748
|
C | CA | 34 | a0001c0001t0001g0206a0001c0001t0002g0006a0001c0001t0002g0015others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52-5284dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910748 | |||||
| chr1:77910748
|
C | CAA | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(18): Show | 21 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-52-5285_-52-5284d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910748 | |||||
| chr1:77910761
|
A | AAAC | 22 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(19): Show | 22 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-52-5292_-52-5291i others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910761 | |||||
| chr1:77910762
|
A | AAC | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52-5292_-52-5291i others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910762 | |||||
| chr1:77910762
|
A | AC | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(38): Show | 44 | HG00438.hp1 HG01496.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-5293_-52-5292i others(3): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910762 | ||||||
| chr1:77910763
|
A | C | 1 | a0001c0001t0003g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-52-5292A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910763 | ||||||
| chr1:77911045
|
C | T | 3 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0221 | 3 | HG01934.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-52-5010C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911045 | ||||||
| chr1:77911132
|
C | T | 1 | a0001c0001t0005g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52-4923C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911132 | ||||||
| chr1:77911485
|
G | A | 1 | a0002c0002t0001g0214 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-52-4570G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911485 | ||||||
| chr1:77911570
|
C | T | 2 | a0001c0001t0005g0179a0001c0001t0017g0168 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-52-4485C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911570 | ||||||
| chr1:77911664
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-52-4391A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911664 | ||||||
| chr1:77911691
|
A | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-4364A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911691 | ||||||
| chr1:77911739
|
T | A | 5 | a0001c0001t0002g0154a0001c0001t0002g0157a0001c0001t0002g0197others(2): Show | 5 | HG00609.hp1 HG02132.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-4316T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911739 | ||||||
| chr1:77911739
|
T | TTA | 24 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0024others(21): Show | 25 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52-4295_-52-4294d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | |||||
| chr1:77911739
|
TTA | T | 34 | a0001c0001t0001g0018a0001c0001t0001g0081a0001c0001t0001g0094others(31): Show | 35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52-4295_-52-4294d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | |||||
| chr1:77911739
|
TTATA | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(151): Show | 158 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-52-4297_-52-4294d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | |||||
| chr1:77911857
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0071a0001c0001t0003g0072others(2): Show | 5 | HG00438.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-4198C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911857 | ||||||
| chr1:77911867
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0123 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-52-4188G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911867 | ||||||
| chr1:77911908
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-52-4147G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911908 | ||||||
| chr1:77911936
|
G | T | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-4119G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911936 | ||||||
| chr1:77911965
|
G | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-4090G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911965 | ||||||
| chr1:77912003
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02976.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-52-4052C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912003 | ||||||
| chr1:77912004
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-52-4051G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912004 | ||||||
| chr1:77912052
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-4003C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912052 | ||||||
| chr1:77912078
|
C | CA | 15 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0114others(12): Show | 15 | HG00621.hp2 HG01175.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-52-3960dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912078 | |||||
| chr1:77912168
|
T | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0027others(20): Show | 24 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52-3887T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912168 | ||||||
| chr1:77912213
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0118 | 3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-52-3842A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912213 | ||||||
| chr1:77912221
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52-3834A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912221 | ||||||
| chr1:77912246
|
A | ATGTGGAA others(4): Show |
2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52-3806_-52-3796d others(13): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912246 | |||||
| chr1:77912295
|
T | C | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-52-3760T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912295 | ||||||
| chr1:77912378
|
TC | T | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-3675delC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912378 | |||||
| chr1:77912596
|
T | TA | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-3456dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912596 | |||||
| chr1:77912718
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0008t0001g0068others(1): Show | 4 | HG01257.hp2 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-3337T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912718 | ||||||
| chr1:77913152
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52-2903C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913152 | ||||||
| chr1:77913162
|
C | T | 3 | a0001c0008t0001g0068a0001c0009t0012g0165a0006c0004t0001g0064 | 3 | HG02145.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-2893C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913162 | ||||||
| chr1:77913202
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52-2853G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913202 | ||||||
| chr1:77913244
|
A | G | 1 | a0002c0002t0001g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-52-2811A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913244 | ||||||
| chr1:77913371
|
T | C | 1 | a0002c0002t0001g0226 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52-2684T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913371 | ||||||
| chr1:77913414
|
C | CA | 8 | a0001c0001t0001g0115a0001c0003t0004g0159a0001c0003t0004g0161others(5): Show | 8 | HG02071.hp1 HG02818.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2628dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77913414 | |||||
| chr1:77913721
|
T | G | 1 | a0001c0001t0002g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-52-2334T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913721 | ||||||
| chr1:77913815
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-52-2240C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913815 | ||||||
| chr1:77914074
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-1981T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914074 | ||||||
| chr1:77914116
|
T | G | 3 | a0001c0008t0001g0068a0001c0009t0012g0165a0006c0004t0001g0064 | 3 | HG02145.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-1939T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914116 | ||||||
| chr1:77914857
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(3): Show | 6 | HG00639.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-1183dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77914857 | |||||
| chr1:77914948
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-52-1107T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914948 | ||||||
| chr1:77915001
|
C | G | 1 | a0001c0001t0004g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-52-1054C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915001 | ||||||
| chr1:77915367
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-52-688T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915367 | ||||||
| chr1:77915425
|
T | G | 1 | a0001c0001t0010g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-52-630T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915425 | ||||||
| chr1:77915664
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-52-391A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915664 | ||||||
| chr1:77916290
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.27+157C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916290 | ||||||
| chr1:77916314
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+181C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916314 | ||||||
| chr1:77916333
|
T | C | 6 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+200T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916333 | ||||||
| chr1:77916353
|
A | C | 24 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(21): Show | 24 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.27+220A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916353 | ||||||
| chr1:77916907
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-659C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916907 | ||||||
| chr1:77917475
|
AT | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-85delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 77917475 | |||||
| chr1:77917782
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.219+25G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 3/12 | chr1 | 77917782 | ||||||
| chr1:77918378
|
A | G | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+105A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918378 | ||||||
| chr1:77918473
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.447+200C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918473 | ||||||
| chr1:77918668
|
G | GA | 10 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0003g0100others(7): Show | 10 | HG02056.hp1 HG02071.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.447+413dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77918668 | |||||
| chr1:77918668
|
GA | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0042others(35): Show | 39 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.447+413delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77918668 | |||||
| chr1:77918772
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0118 | 3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.447+499T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918772 | ||||||
| chr1:77918824
|
T | C | 1 | a0001c0001t0006g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.447+551T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918824 | ||||||
| chr1:77918833
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+560C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918833 | ||||||
| chr1:77919075
|
G | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.447+802G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919075 | ||||||
| chr1:77919302
|
G | A | 1 | a0002c0002t0001g0233 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.447+1029G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919302 | ||||||
| chr1:77919318
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.447+1045A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919318 | ||||||
| chr1:77919582
|
A | AT | 49 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0025others(46): Show | 52 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.447+1327dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77919582 | |||||
| chr1:77919582
|
AT | A | 7 | a0001c0001t0001g0042a0001c0003t0004g0159a0001c0003t0004g0161others(4): Show | 7 | HG02698.hp1 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+1327delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77919582 | |||||
| chr1:77919644
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.447+1371C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919644 | ||||||
| chr1:77919784
|
G | C | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+1511G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919784 | ||||||
| chr1:77919845
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.447+1572C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919845 | ||||||
| chr1:77919925
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.447+1652A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919925 | ||||||
| chr1:77919930
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0042others(29): Show | 33 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.447+1657C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919930 | ||||||
| chr1:77920024
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0244others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1751C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920024 | ||||||
| chr1:77920153
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.447+1880G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920153 | ||||||
| chr1:77920181
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0071a0001c0001t0003g0072others(2): Show | 5 | HG00438.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1908C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920181 | ||||||
| chr1:77920364
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.447+2091A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920364 | ||||||
| chr1:77920489
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2216C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920489 | ||||||
| chr1:77920555
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0207 | 2 | HG00639.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.447+2282A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920555 | ||||||
| chr1:77920619
|
T | TA | 10 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0135others(7): Show | 10 | HG01109.hp2 HG01168.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.447+2369dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | |||||
| chr1:77920619
|
TA | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.447+2369delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | |||||
| chr1:77920619
|
TAA | T | 13 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0061others(10): Show | 13 | HG00323.hp1 HG01256.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2368_447+2369d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | |||||
| chr1:77920619
|
TAAAAAAA others(5): Show |
T | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2358_447+2369d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | |||||
| chr1:77920800
|
G | T | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2527G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920800 | ||||||
| chr1:77920804
|
GAGA | G | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.447+2534_447+2536d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920804 | |||||
| chr1:77920938
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+2665C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920938 | ||||||
| chr1:77921081
|
A | C | 1 | a0001c0009t0012g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.447+2808A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921081 | ||||||
| chr1:77921124
|
A | G | 1 | a0002c0002t0001g0226 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.447+2851A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921124 | ||||||
| chr1:77921242
|
T | C | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2969T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921242 | ||||||
| chr1:77921316
|
C | T | 5 | a0002c0002t0001g0220a0002c0002t0001g0225a0002c0002t0001g0229others(2): Show | 5 | NA18947.hp1 NA18969.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+3043C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921316 | ||||||
| chr1:77921585
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.447+3312C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921585 | ||||||
| chr1:77921810
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.448-3378C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921810 | ||||||
| chr1:77921860
|
G | A | 4 | a0001c0001t0005g0155a0001c0001t0005g0179a0001c0001t0010g0151others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3328G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921860 | ||||||
| chr1:77922013
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.448-3175C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922013 | ||||||
| chr1:77922140
|
CT | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.448-3031delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77922140 | |||||
| chr1:77922344
|
T | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.448-2844T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922344 | ||||||
| chr1:77922409
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.448-2779G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922409 | ||||||
| chr1:77922420
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.448-2768C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922420 | ||||||
| chr1:77922584
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.448-2604C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922584 | ||||||
| chr1:77922597
|
T | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2591T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922597 | ||||||
| chr1:77922601
|
C | CT | 36 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(33): Show | 39 | HG00438.hp1 HG00735.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.448-2573dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77922601 | |||||
| chr1:77922616
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2572G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922616 | ||||||
| chr1:77922618
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2570G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922618 | ||||||
| chr1:77922762
|
A | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-2426A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922762 | ||||||
| chr1:77923003
|
C | CT | 30 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0031others(27): Show | 30 | HG01106.hp1 HG01109.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.448-2163dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923003 | |||||
| chr1:77923056
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.448-2132C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923056 | ||||||
| chr1:77923060
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.448-2128C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923060 | ||||||
| chr1:77923147
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-2041C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923147 | ||||||
| chr1:77923160
|
A | AT | 72 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(69): Show | 75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.448-2009dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923160 | |||||
| chr1:77923160
|
A | ATT | 5 | a0001c0001t0001g0037a0001c0001t0003g0103a0001c0001t0004g0255others(2): Show | 5 | HG00642.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-2010_448-2009d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923160 | |||||
| chr1:77923195
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.448-1993C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923195 | ||||||
| chr1:77923214
|
G | C | 4 | a0001c0001t0005g0155a0001c0001t0005g0179a0001c0001t0010g0151others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-1974G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923214 | ||||||
| chr1:77923253
|
C | A | 1 | a0001c0001t0002g0184 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.448-1935C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923253 | ||||||
| chr1:77923467
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448-1721A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923467 | ||||||
| chr1:77923679
|
CT | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(197): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.448-1489delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923679 | |||||
| chr1:77923867
|
G | A | 6 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1321G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923867 | ||||||
| chr1:77924019
|
G | A | 6 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0016others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-1169G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924019 | ||||||
| chr1:77924097
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0014g0204 | 3 | HG02258.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.448-1091C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924097 | ||||||
| chr1:77924135
|
G | A | 1 | a0002c0002t0001g0233 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.448-1053G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924135 | ||||||
| chr1:77924144
|
T | C | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1044T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924144 | ||||||
| chr1:77924348
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.448-840C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924348 | ||||||
| chr1:77924361
|
C | CA | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.448-816dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77924361 | |||||
| chr1:77924476
|
G | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.448-712G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924476 | ||||||
| chr1:77924666
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.448-522T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924666 | ||||||
| chr1:77924667
|
C | CT | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.448-514dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77924667 | |||||
| chr1:77924667
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0077 | 2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.448-521C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924667 | ||||||
| chr1:77924705
|
A | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.448-483A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924705 | ||||||
| chr1:77924744
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.448-444G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924744 | ||||||
| chr1:77925335
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0065others(7): Show | 10 | HG01993.hp1 HG02132.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+106T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 6/12 | chr1 | 77925335 | ||||||
| chr1:77925591
|
C | T | 4 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0002t0001g0217others(1): Show | 4 | HG01934.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+362C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 6/12 | chr1 | 77925591 | ||||||
| chr1:77926935
|
T | G | 1 | a0001c0001t0004g0116 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.864+43T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77926935 | ||||||
| chr1:77927123
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+231A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927123 | ||||||
| chr1:77927182
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.864+290C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927182 | ||||||
| chr1:77927186
|
A | G | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.864+294A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927186 | ||||||
| chr1:77927197
|
C | T | 1 | a0001c0001t0005g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.864+305C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927197 | ||||||
| chr1:77927259
|
A | T | 1 | a0001c0001t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.864+367A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927259 | ||||||
| chr1:77927391
|
A | G | 5 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(2): Show | 5 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+499A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927391 | ||||||
| chr1:77927599
|
T | A | 1 | a0001c0001t0001g0123 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.864+707T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927599 | ||||||
| chr1:77927600
|
GTC | G | 13 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(10): Show | 13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+710_864+711del others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 77927600 | |||||
| chr1:77927601
|
T | TGA | 6 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0060others(3): Show | 6 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+709_864+710ins others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927601 | ||||||
| chr1:77927602
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.864+710C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927602 | ||||||
| chr1:77927603
|
T | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.864+711T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927603 | ||||||
| chr1:77927603
|
T | TGA | 12 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(9): Show | 12 | HG02280.hp1 HG02809.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.864+712_864+713ins others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 77927603 | |||||
| chr1:77927604
|
G | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0060others(3): Show | 6 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+712G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927604 | ||||||
| chr1:77927605
|
T | A | 13 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(10): Show | 13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+713T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927605 | ||||||
| chr1:77927606
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(190): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.864+714G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927606 | ||||||
| chr1:77927607
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.864+715T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927607 | ||||||
| chr1:77927608
|
G | C | 13 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(10): Show | 13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+716G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927608 | ||||||
| chr1:77927610
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.864+718G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927610 | ||||||
| chr1:77927614
|
G | T | 6 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+722G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927614 | ||||||
| chr1:77927732
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG00621.hp1 HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.864+840G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927732 | ||||||
| chr1:77927769
|
T | C | 1 | a0001c0001t0003g0070 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.864+877T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927769 | ||||||
| chr1:77927936
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.864+1044T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927936 | ||||||
| chr1:77927987
|
G | T | 1 | a0001c0001t0002g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.864+1095G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927987 | ||||||
| chr1:77927988
|
A | T | 1 | a0001c0001t0002g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.864+1096A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927988 | ||||||
| chr1:77928053
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.864+1161A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928053 | ||||||
| chr1:77928068
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.864+1176G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928068 | ||||||
| chr1:77928137
|
T | C | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-1179T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928137 | ||||||
| chr1:77928236
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.865-1080G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928236 | ||||||
| chr1:77928254
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0237 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.865-1062C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928254 | ||||||
| chr1:77928708
|
A | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.865-608A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928708 | ||||||
| chr1:77928773
|
G | A | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-543G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928773 | ||||||
| chr1:77928866
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.865-450C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928866 | ||||||
| chr1:77928901
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.865-415C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928901 | ||||||
| chr1:77928944
|
G | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.865-372G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928944 | ||||||
| chr1:77929312
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.865-4T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77929312 | ||||||
| chr1:77929632
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1053+128T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929632 | ||||||
| chr1:77929717
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1053+213C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929717 | ||||||
| chr1:77929877
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1053+373C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929877 | ||||||
| chr1:77930333
|
T | A | 1 | a0001c0001t0002g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1053+829T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930333 | ||||||
| chr1:77930654
|
GCT | G | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+1153_1053+115 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77930654 | |||||
| chr1:77930773
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1053+1269A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930773 | ||||||
| chr1:77930784
|
C | T | 2 | a0001c0008t0001g0068a0006c0004t0001g0064 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1053+1280C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930784 | ||||||
| chr1:77930941
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1053+1437T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930941 | ||||||
| chr1:77931109
|
C | T | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+1605C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931109 | ||||||
| chr1:77931158
|
C | T | 1 | a0001c0001t0005g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1053+1654C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931158 | ||||||
| chr1:77931231
|
C | CA | 10 | a0001c0001t0001g0035a0001c0001t0002g0015a0001c0001t0002g0148others(7): Show | 10 | HG00741.hp2 HG01106.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+1760dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CA | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0143others(16): Show | 19 | HG00609.hp1 HG00735.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1053+1760delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAA | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(12): Show | 15 | HG00639.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1053+1759_1053+176 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAA | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0137a0001c0001t0004g0253others(5): Show | 8 | HG02300.hp2 HG02615.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1053+1758_1053+176 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAA | C | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(19): Show | 22 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1053+1757_1053+176 others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAA | C | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(15): Show | 21 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1053+1756_1053+176 others(9): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1053+1750_1053+176 others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1053+1748_1053+176 others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0029a0001c0001t0005g0189 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1053+1746_1053+176 others(19): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053+1745_1053+176 others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(11): Show |
C | 15 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0060others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053+1743_1053+176 others(22): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931231
|
CAAAAAAA others(12): Show |
C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(120): Show | 126 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1053+1742_1053+176 others(23): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | |||||
| chr1:77931412
|
CA | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0077a0001c0001t0001g0081others(18): Show | 22 | HG00438.hp2 HG01106.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1054-1841delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931412
|
CAA | C | 45 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0026others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1054-1842_1054-184 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931412
|
CAAA | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 128 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.1054-1843_1054-184 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931412
|
CAAAA | C | 34 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0032others(31): Show | 37 | HG00438.hp1 HG01261.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1054-1844_1054-184 others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931412
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-1850_1054-184 others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931412
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0231 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1054-1854_1054-184 others(18): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | |||||
| chr1:77931506
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1054-1776C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931506 | ||||||
| chr1:77931670
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1054-1612T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931670 | ||||||
| chr1:77931856
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1054-1426C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931856 | ||||||
| chr1:77932028
|
C | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1054-1254C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932028 | ||||||
| chr1:77932429
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1054-853C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932429 | ||||||
| chr1:77932692
|
ATTTC | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-586_1054-583d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77932692 | |||||
| chr1:77932894
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1054-388G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932894 | ||||||
| chr1:77933046
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-236A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77933046 | ||||||
| chr1:77933076
|
G | A | 2 | a0001c0003t0009g0162a0001c0003t0009g0164 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1054-206G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77933076 | ||||||
| chr1:77933522
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1251+43C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933522 | ||||||
| chr1:77933527
|
T | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1251+48T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933527 | ||||||
| chr1:77933581
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1251+102A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933581 | ||||||
| chr1:77933910
|
ACTGCAGC others(32): Show |
A | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1251+434_1251+472d others(41): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77933910 | |||||
| chr1:77934011
|
A | AT | 15 | a0001c0001t0001g0010a0001c0001t0002g0194a0001c0001t0002g0195others(12): Show | 15 | HG01496.hp2 HG02451.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1251+548dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934011
|
A | ATTTTTT | 33 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0001t0004g0075others(30): Show | 34 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1251+543_1251+548d others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934011
|
A | ATTTTTTT | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(96): Show | 101 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1251+542_1251+548d others(9): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934011
|
A | ATTTTTTT others(1): Show |
58 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(55): Show | 61 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1251+541_1251+548d others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934011
|
A | ATTTTTTT others(2): Show |
15 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0039others(12): Show | 15 | HG00438.hp1 HG00735.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1251+540_1251+548d others(11): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934011
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1251+539_1251+548d others(12): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | |||||
| chr1:77934048
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1251+569T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934048 | ||||||
| chr1:77934163
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+684C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934163 | ||||||
| chr1:77934164
|
GATGCCCG others(1021): Show |
G | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1251+711_1252-606d others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934164 | |||||
| chr1:77934166
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251+687T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934166 | ||||||
| chr1:77934190
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1251+711G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934190 | ||||||
| chr1:77934230
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1251+751G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934230 | ||||||
| chr1:77934307
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1251+828G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934307 | ||||||
| chr1:77934413
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0065others(7): Show | 10 | HG01993.hp1 HG02132.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+934G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934413 | ||||||
| chr1:77934468
|
A | C | 3 | a0001c0003t0004g0163a0001c0003t0009g0162a0001c0003t0009g0164 | 3 | HG02818.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1251+989A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934468 | ||||||
| chr1:77934813
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1252-1010T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934813 | ||||||
| chr1:77934855
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0023others(78): Show | 83 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1252-968A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934855 | ||||||
| chr1:77934910
|
T | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-913T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934910 | ||||||
| chr1:77934912
|
T | C | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-911T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934912 | ||||||
| chr1:77934913
|
G | T | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-910G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934913 | ||||||
| chr1:77934917
|
G | T | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-906G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934917 | ||||||
| chr1:77934918
|
A | C | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-905A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934918 | ||||||
| chr1:77934919
|
C | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-904C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934919 | ||||||
| chr1:77935265
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1252-558C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935265 | ||||||
| chr1:77935522
|
T | C | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(38): Show | 44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1252-301T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935522 | ||||||
| chr1:77935582
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1252-241T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935582 | ||||||
| chr1:77936156
|
ATACAG | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+115_1473+119d others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77936156 | |||||
| chr1:77936308
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1473+264C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936308 | ||||||
| chr1:77936581
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1473+537G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936581 | ||||||
| chr1:77936602
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1473+558G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936602 | ||||||
| chr1:77936966
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1473+922A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936966 | ||||||
| chr1:77936970
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(244): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.1473+926C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936970 | ||||||
| chr1:77937080
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1473+1036T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937080 | ||||||
| chr1:77937082
|
GGTGGGTC others(6): Show |
G | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1473+1040_1473+105 others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77937082 | |||||
| chr1:77937154
|
A | G | 3 | a0002c0002t0001g0242a0002c0002t0001g0243a0002c0002t0001g0251 | 3 | HG00642.hp2 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1473+1110A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937154 | ||||||
| chr1:77937166
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1473+1122C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937166 | ||||||
| chr1:77937245
|
G | A | 1 | a0001c0001t0010g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1473+1201G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937245 | ||||||
| chr1:77937259
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1473+1215G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937259 | ||||||
| chr1:77937400
|
T | TA | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(38): Show | 44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+1357dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77937400 | |||||
| chr1:77937427
|
G | A | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(38): Show | 44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+1383G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937427 | ||||||
| chr1:77937452
|
G | A | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+1408G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937452 | ||||||
| chr1:77937460
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1473+1416T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937460 | ||||||
| chr1:77937487
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1473+1443C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937487 | ||||||
| chr1:77937596
|
G | A | 6 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0001t0002g0157others(3): Show | 6 | HG00609.hp1 HG00738.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+1552G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937596 | ||||||
| chr1:77937666
|
G | C | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1622G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937666 | ||||||
| chr1:77937668
|
G | GCAGCACA others(32): Show |
1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1624_1473+162 others(43): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937668 | ||||||
| chr1:77937672
|
G | A | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1628G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937672 | ||||||
| chr1:77937675
|
C | A | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1631C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937675 | ||||||
| chr1:77937675
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1473+1631C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937675 | ||||||
| chr1:77937693
|
A | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1473+1649A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937693 | ||||||
| chr1:77938131
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1473+2087G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938131 | ||||||
| chr1:77938171
|
T | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1473+2127T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938171 | ||||||
| chr1:77938230
|
A | G | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+2186A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938230 | ||||||
| chr1:77938487
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2443A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938487 | ||||||
| chr1:77938513
|
G | A | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+2469G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938513 | ||||||
| chr1:77938523
|
T | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG00639.hp2 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+2479T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938523 | ||||||
| chr1:77938589
|
CA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1473+2563delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938589 | |||||
| chr1:77938589
|
CAA | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1473+2562_1473+256 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938589 | |||||
| chr1:77938618
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2574A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938618 | ||||||
| chr1:77938643
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1473+2599A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938643 | ||||||
| chr1:77938659
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2615T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938659 | ||||||
| chr1:77938666
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2622A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938666 | ||||||
| chr1:77938722
|
CAAG | C | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(38): Show | 44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+2682_1473+268 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938722 | |||||
| chr1:77938802
|
A | C | 1 | a0001c0001t0004g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1473+2758A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938802 | ||||||
| chr1:77939244
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1474-2779G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939244 | ||||||
| chr1:77939256
|
G | A | 10 | a0001c0001t0002g0149a0001c0001t0002g0170a0001c0001t0002g0171others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-2767G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939256 | ||||||
| chr1:77939541
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG00621.hp1 HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1474-2482T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939541 | ||||||
| chr1:77939749
|
T | C | 22 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0027others(19): Show | 23 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.1474-2274T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939749 | ||||||
| chr1:77939771
|
G | GT | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-2251dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77939771 | |||||
| chr1:77939799
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1474-2224G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939799 | ||||||
| chr1:77939848
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1474-2175C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939848 | ||||||
| chr1:77939931
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1474-2092G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939931 | ||||||
| chr1:77940113
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1474-1910T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940113 | ||||||
| chr1:77940270
|
C | A | 1 | a0001c0009t0012g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1474-1753C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940270 | ||||||
| chr1:77940428
|
G | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(26): Show | 32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1474-1595G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940428 | ||||||
| chr1:77940750
|
A | G | 6 | a0001c0003t0004g0159a0001c0003t0004g0161a0001c0003t0004g0163others(3): Show | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-1273A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940750 | ||||||
| chr1:77940816
|
T | C | 1 | a0001c0001t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1474-1207T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940816 | ||||||
| chr1:77940820
|
GT | G | 6 | a0001c0001t0005g0019a0001c0001t0005g0150a0001c0001t0005g0155others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474-1201delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77940820 | |||||
| chr1:77940831
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1474-1192C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940831 | ||||||
| chr1:77940946
|
T | C | 1 | a0001c0001t0016g0009 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1474-1077T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940946 | ||||||
| chr1:77941229
|
TAGAAACC others(8): Show |
T | 86 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0148others(83): Show | 90 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1474-777_1474-763d others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77941229 | |||||
| chr1:77941246
|
G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0025others(7): Show | 11 | HG01099.hp2 HG01175.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-777G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77941246 | ||||||
| chr1:77941824
|
C | CT | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1474-198dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77941824 | |||||
| chr1:77941946
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1474-77A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77941946 | ||||||
| chr1:77942370
|
TA | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660-80delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 77942370 |