Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4676 |
|---|---|
| ensemblid | ENSG00000205531.14 |
| hgncid | 7640 |
| symbol | NAP1L4 |
| name | nucleosome assembly protein 1 like 4 |
| refseq_nuc | NM_005969.4 |
| refseq_prot | NP_005960.1 |
| ensembl_nuc | ENST00000380542.9 |
| ensembl_prot | ENSP00000369915.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 2944437 |
| end | 2992329 |
| strand | - |
| ver | v1.2 |
| region | chr11:2944437-2992329 |
| region5000 | chr11:2939437-2997329 |
| regionname0 | NAP1L4_chr11_2944437_2992329 |
| regionname5000 | NAP1L4_chr11_2939437_2997329 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 375 | 329 | 95 | 51 | 124 | 16 | 42 | 102 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0002 | 0/0 | 375 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0003 | 0/0 | 194 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0004 | 0/0 | 375 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1128 | 312 | 83 | 49 | 123 | 15 | 41 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0002 | 0/0 | 1128 | 10 | 10 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0003 | 0/0 | 1128 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0004 | 0/0 | 1128 | 4 | 0 | 2 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0005 | 0/0 | 1128 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0006 | 0/0 | 1128 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0007 | 0/0 | 1138 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| c0008 | 0/0 | 1128 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1336 | 204 | 74 | 32 | 62 | 10 | 26 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0002 | 0/1 | 1336 | 103 | 5 | 19 | 60 | 4 | 14 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0003 | 0/0 | 1336 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0004 | 0/0 | 1336 | 4 | 2 | 0 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0005 | 0/0 | 1336 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0006 | 0/0 | 1336 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0007 | 0/0 | 1336 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0008 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0009 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0010 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0011 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0012 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0013 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0014 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| t0015 | 0/0 | 1325 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0003 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1128 | 312 | 83 | 49 | 123 | 15 | 41 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0002 | 0/0 | 1128 | 10 | 10 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0004 | 0/0 | 1128 | 4 | 0 | 2 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0005 | 0/0 | 1128 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0006 | 0/0 | 1128 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0002c0003 | 0/0 | 1128 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0003c0007 | 0/0 | 1138 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0004c0008 | 0/0 | 1128 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2463 | 192 | 69 | 29 | 60 | 9 | 25 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0002 | 0/1 | 2463 | 102 | 5 | 19 | 59 | 4 | 14 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0004 | 0/0 | 2463 | 4 | 2 | 0 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0005 | 0/0 | 2463 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0006 | 0/0 | 2463 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0008 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0009 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0010 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0011 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0012 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0013 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0001t0014 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0002t0003 | 0/0 | 2463 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0002t0007 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0002t0015 | 0/0 | 2452 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0004t0001 | 0/0 | 2463 | 4 | 0 | 2 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0005t0001 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0001c0006t0001 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0002c0003t0001 | 0/0 | 2463 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0003c0007t0001 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| a0004c0008t0002 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | copy fasta | chr11 | 2939437 | 2997329 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0012g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0015g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0003c0007t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0004c0008t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0253 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0026 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0023 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0154 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0113 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0209 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0053 | EAS | CDX | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02280 | hp1 | a0001 | c0002 | t0015 | g0277 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0270 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0271 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0015 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0116 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02886 | hp2 | a0001 | c0002 | t0007 | g0015 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0114 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0111 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0115 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0206 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0235 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18947 | hp1 | a0001 | c0006 | t0001 | g0240 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18980 | hp1 | a0004 | c0008 | t0002 | g0072 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19076 | hp1 | a0003 | c0007 | t0001 | g0119 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ASW | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0198 | AFR | ASW | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20752 | hp2 | a0001 | c0001 | t0014 | g0190 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0079 | REF | REF | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2959858
|
C | T | 1 | a0002 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.658G>A | p.Val220Ile | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/16 | 751/2463 | 658/1128 | 220/375 | chr11 | 2959858 | ||
| chr11:2964706
|
T | TCACTTTA others(3): Show |
1 | a0003 | 1 | NA19076.hp1 | frameshift_variant&stop_gained | HIGH | c.570_579dupTATTAAAG others(2): Show |
p.Lys194fs | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/16 | 672/2463 | 579/1128 | 193/375 | chr11 | 2964706 | ||
| chr11:2969894
|
G | A | 1 | a0004 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.443C>T | p.Ala148Val | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/16 | 536/2463 | 443/1128 | 148/375 | chr11 | 2969894 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2951274
|
C | T | 1 | a0001c0006 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.1107G>A | p.Ala369Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/16 | 1200/2463 | 1107/1128 | 369/375 | chr11 | 2951274 | ||
| chr11:2954569
|
A | C | 1 | a0002c0003 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.993T>G | p.Ala331Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/16 | 1086/2463 | 993/1128 | 331/375 | chr11 | 2954569 | ||
| chr11:2971517
|
G | A | 1 | a0001c0002 | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
synonymous_variant | LOW | c.333C>T | p.Thr111Thr | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/16 | 426/2463 | 333/1128 | 111/375 | chr11 | 2971517 | ||
| chr11:2972123
|
T | C | 1 | a0001c0004 | 4 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
synonymous_variant | LOW | c.294A>G | p.Leu98Leu | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/16 | 387/2463 | 294/1128 | 98/375 | chr11 | 2972123 | ||
| chr11:2978294
|
T | G | 1 | a0001c0005 | 2 | HG02055.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.63A>C | p.Ala21Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/16 | 156/2463 | 63/1128 | 21/375 | chr11 | 2978294 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2944498
|
T | A | 1 | a0001c0001t0004 | 4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1181A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4761 | chr11 | 2944498 | |||||
| chr11:2944554
|
T | G | 1 | a0001c0002t0007 | 2 | HG02630.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4705 | chr11 | 2944554 | |||||
| chr11:2944607
|
CCCACCCA others(4): Show |
C | 1 | a0001c0002t0015 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1061_*1071delCTGG others(7): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4641 | chr11 | 2944607 | |||||
| chr11:2944707
|
C | T | 1 | a0001c0001t0009 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4552 | chr11 | 2944707 | |||||
| chr11:2944791
|
G | A | 3 | a0001c0002t0003a0001c0002t0007a0001c0002t0015 | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*888C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4468 | chr11 | 2944791 | |||||
| chr11:2944948
|
A | T | 1 | a0001c0001t0008 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4311 | chr11 | 2944948 | |||||
| chr11:2945063
|
C | G | 3 | a0001c0001t0002a0001c0001t0012a0004c0008t0002 | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*616G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4196 | chr11 | 2945063 | |||||
| chr11:2945283
|
T | C | 1 | a0001c0001t0010 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3976 | chr11 | 2945283 | |||||
| chr11:2945374
|
G | A | 1 | a0001c0001t0011 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*305C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3885 | chr11 | 2945374 | |||||
| chr11:2945404
|
T | C | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3855 | chr11 | 2945404 | |||||
| chr11:2945496
|
G | A | 1 | a0001c0001t0013 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3763 | chr11 | 2945496 | |||||
| chr11:2945592
|
C | A | 1 | a0001c0001t0014 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3667 | chr11 | 2945592 | |||||
| chr11:2992265
|
T | C | 1 | a0001c0001t0006 | 3 | NA18987.hp2 NA18993.hp1 NA19007.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13045 | chr11 | 2992265 | |||||
| chr11:2992299
|
T | C | 1 | a0001c0002t0015 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13079 | chr11 | 2992299 | |||||
| chr11:2992315
|
G | C | 1 | a0001c0001t0005 | 4 | HG00642.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-79C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13095 | chr11 | 2992315 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2945653
|
A | G | 1 | a0001c0005t0001g0209 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.*33-7T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945653 | ||||||
| chr11:2945766
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(21): Show | 31 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.*33-120A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945766 | ||||||
| chr11:2945775
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*33-129T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945775 | ||||||
| chr11:2945819
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*33-173G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945819 | ||||||
| chr11:2945834
|
AG | A | 3 | a0002c0003t0001g0026a0002c0003t0001g0270a0002c0003t0001g0271 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.*33-189delC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945834 | ||||||
| chr11:2945837
|
G | GT | 6 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0144others(3): Show | 6 | HG03017.hp1 NA18978.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.*33-192dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945837 | ||||||
| chr11:2945937
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.*33-291G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945937 | ||||||
| chr11:2946018
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*33-372T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946018 | ||||||
| chr11:2946094
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.*33-448C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946094 | ||||||
| chr11:2946114
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*33-468A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946114 | ||||||
| chr11:2946172
|
C | T | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*33-526G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946172 | ||||||
| chr11:2946213
|
A | C | 1 | a0001c0001t0002g0083 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.*33-567T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946213 | ||||||
| chr11:2946223
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*33-577G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946223 | ||||||
| chr11:2946320
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*33-674C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946320 | ||||||
| chr11:2946671
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.*33-1025G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946671 | ||||||
| chr11:2946745
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.*33-1099T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946745 | ||||||
| chr11:2946842
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*33-1196C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946842 | ||||||
| chr11:2946968
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0135 | 4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*33-1322G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946968 | ||||||
| chr11:2947123
|
T | C | 6 | a0001c0002t0003g0014a0001c0002t0003g0112a0001c0002t0003g0113others(3): Show | 8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.*33-1477A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947123 | ||||||
| chr11:2947219
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*33-1573G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947219 | ||||||
| chr11:2947279
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(22): Show | 32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33-1633G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947279 | ||||||
| chr11:2947280
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(22): Show | 32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33-1634C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947280 | ||||||
| chr11:2947316
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.*33-1670A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947316 | ||||||
| chr11:2947344
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*33-1698A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947344 | ||||||
| chr11:2947417
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*33-1771G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947417 | ||||||
| chr11:2947517
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.*32+1710A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947517 | ||||||
| chr11:2947579
|
A | G | 94 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0001g0159others(91): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.*32+1648T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947579 | ||||||
| chr11:2947616
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.*32+1611G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947616 | ||||||
| chr11:2947618
|
G | GA | 6 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32+1608dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947618 | ||||||
| chr11:2947619
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.*32+1608T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947619 | ||||||
| chr11:2947704
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*32+1523G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947704 | ||||||
| chr11:2947752
|
CAACT | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32+1471_*32+1474d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947752 | ||||||
| chr11:2947780
|
C | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.*32+1447G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947780 | ||||||
| chr11:2947813
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.*32+1414T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947813 | ||||||
| chr11:2947882
|
G | A | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.*32+1345C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947882 | ||||||
| chr11:2947892
|
C | T | 7 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(4): Show | 9 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.*32+1335G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947892 | ||||||
| chr11:2948012
|
G | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(52): Show | 66 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.*32+1215C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948012 | ||||||
| chr11:2948049
|
A | G | 7 | a0001c0001t0002g0012a0001c0001t0002g0036a0001c0001t0002g0039others(4): Show | 8 | HG00621.hp1 HG01123.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.*32+1178T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948049 | ||||||
| chr11:2948068
|
A | AG | 279 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(276): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.*32+1158dupC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948068 | ||||||
| chr11:2948121
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*32+1106C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948121 | ||||||
| chr11:2948227
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.*32+1000T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948227 | ||||||
| chr11:2948300
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*32+927T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948300 | ||||||
| chr11:2948463
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*32+764C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948463 | ||||||
| chr11:2948474
|
G | A | 1 | a0001c0001t0002g0013 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.*32+753C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948474 | ||||||
| chr11:2948485
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*32+742C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948485 | ||||||
| chr11:2948490
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.*32+737C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948490 | ||||||
| chr11:2948541
|
G | A | 84 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(81): Show | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.*32+686C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948541 | ||||||
| chr11:2948542
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(11): Show | 20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*32+685G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948542 | ||||||
| chr11:2948666
|
C | T | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*32+561G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948666 | ||||||
| chr11:2948668
|
G | A | 1 | a0001c0005t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*32+559C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948668 | ||||||
| chr11:2948802
|
GT | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0135 | 4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*32+424delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948802 | ||||||
| chr11:2948910
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(11): Show | 20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*32+317G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948910 | ||||||
| chr11:2949031
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0064 | 2 | HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.*32+196C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2949031 | ||||||
| chr11:2949290
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1123-26T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949290 | ||||||
| chr11:2949348
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1123-84T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949348 | ||||||
| chr11:2949625
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.1123-361T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949625 | ||||||
| chr11:2949635
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(22): Show | 32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1123-371A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949635 | ||||||
| chr11:2949637
|
G | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(22): Show | 32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1123-373C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949637 | ||||||
| chr11:2949649
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(8): Show | 12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123-385G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949649 | ||||||
| chr11:2949663
|
C | T | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1123-399G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949663 | ||||||
| chr11:2949664
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(23): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1123-400C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949664 | ||||||
| chr11:2949759
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0246 | 2 | NA18946.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1123-495G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949759 | ||||||
| chr11:2949760
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1123-496C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949760 | ||||||
| chr11:2949922
|
T | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-658A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949922 | ||||||
| chr11:2950179
|
G | A | 1 | a0001c0001t0011g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1123-915C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950179 | ||||||
| chr11:2950297
|
CA | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(11): Show | 20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1122+961delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950297 | ||||||
| chr11:2950555
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1122+704C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950555 | ||||||
| chr11:2950643
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1122+616A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950643 | ||||||
| chr11:2950848
|
T | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1122+411A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950848 | ||||||
| chr11:2950867
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1122+392G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950867 | ||||||
| chr11:2950948
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1122+311A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950948 | ||||||
| chr11:2951021
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1122+238C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951021 | ||||||
| chr11:2951127
|
T | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0118others(9): Show | 13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+132A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951127 | ||||||
| chr11:2951209
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0139others(24): Show | 31 | HG01261.hp1 HG02698.hp2 HG02738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1122+50G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951209 | ||||||
| chr11:2951234
|
T | C | 1 | a0001c0001t0002g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1122+25A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951234 | ||||||
| chr11:2951357
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1066-42T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951357 | ||||||
| chr11:2951534
|
A | T | 6 | a0001c0001t0002g0034a0001c0001t0002g0045a0001c0001t0002g0046others(3): Show | 6 | NA18964.hp1 NA18973.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066-219T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951534 | ||||||
| chr11:2951545
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1066-230A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951545 | ||||||
| chr11:2951603
|
C | A | 1 | a0001c0001t0002g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1065+177G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951603 | ||||||
| chr11:2951617
|
G | C | 1 | a0001c0002t0003g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065+163C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951617 | ||||||
| chr11:2951669
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1065+111C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951669 | ||||||
| chr11:2951929
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(66): Show | 80 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1036-120C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2951929 | ||||||
| chr11:2951942
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036-133G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2951942 | ||||||
| chr11:2952014
|
G | A | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1036-205C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952014 | ||||||
| chr11:2952094
|
CCCTGGCT others(3): Show |
C | 3 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0135 | 4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036-295_1036-286d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952094 | ||||||
| chr11:2952188
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1036-379C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952188 | ||||||
| chr11:2952320
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1036-511A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952320 | ||||||
| chr11:2952367
|
C | T | 1 | a0001c0001t0002g0013 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1036-558G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952367 | ||||||
| chr11:2952466
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1036-657T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952466 | ||||||
| chr11:2952471
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036-662A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952471 | ||||||
| chr11:2952474
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1036-665A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952474 | ||||||
| chr11:2952510
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1036-701T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952510 | ||||||
| chr11:2952533
|
AT | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1036-725delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952533 | ||||||
| chr11:2952618
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1036-809C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952618 | ||||||
| chr11:2952650
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1036-841C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952650 | ||||||
| chr11:2952666
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1036-857C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952666 | ||||||
| chr11:2952871
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0088 | 2 | NA18950.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1036-1062C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952871 | ||||||
| chr11:2952958
|
C | CTT | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1036-1151_1036-115 others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952958 | ||||||
| chr11:2953127
|
A | C | 5 | a0001c0001t0001g0257a0001c0001t0005g0027a0001c0001t0005g0278others(2): Show | 6 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036-1318T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953127 | ||||||
| chr11:2953366
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0137 | 3 | HG00323.hp2 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1035+1161A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953366 | ||||||
| chr11:2953400
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1035+1127T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953400 | ||||||
| chr11:2953429
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1035+1098T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953429 | ||||||
| chr11:2953581
|
C | A | 1 | a0001c0001t0011g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1035+946G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953581 | ||||||
| chr11:2953682
|
T | C | 83 | a0001c0001t0001g0044a0001c0001t0001g0159a0001c0001t0002g0001others(80): Show | 103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1035+845A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953682 | ||||||
| chr11:2954085
|
T | C | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1035+442A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954085 | ||||||
| chr11:2954262
|
A | G | 1 | a0001c0001t0014g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1035+265T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954262 | ||||||
| chr11:2954352
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1035+175A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954352 | ||||||
| chr11:2954757
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.916-111T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2954757 | ||||||
| chr11:2954818
|
T | C | 1 | a0001c0001t0002g0038 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.916-172A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2954818 | ||||||
| chr11:2955102
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | HG01346.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-456C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955102 | ||||||
| chr11:2955303
|
T | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.915+441A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955303 | ||||||
| chr11:2955322
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.915+422C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955322 | ||||||
| chr11:2955342
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+402C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955342 | ||||||
| chr11:2955350
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.915+394G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955350 | ||||||
| chr11:2955354
|
T | C | 84 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(81): Show | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.915+390A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955354 | ||||||
| chr11:2955362
|
A | AT | 26 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0110others(23): Show | 33 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.915+381dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955362 | ||||||
| chr11:2955481
|
C | T | 55 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(52): Show | 66 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.915+263G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955481 | ||||||
| chr11:2955875
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-109G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2955875 | ||||||
| chr11:2955938
|
A | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.893-172T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2955938 | ||||||
| chr11:2956004
|
GC | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(28): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.893-239delG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956004 | ||||||
| chr11:2956024
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.893-258G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956024 | ||||||
| chr11:2956032
|
G | A | 1 | a0001c0001t0011g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.893-266C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956032 | ||||||
| chr11:2956086
|
G | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.893-320C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956086 | ||||||
| chr11:2956223
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.893-457C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956223 | ||||||
| chr11:2956324
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-558C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956324 | ||||||
| chr11:2956403
|
A | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.893-637T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956403 | ||||||
| chr11:2956447
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893-681T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956447 | ||||||
| chr11:2956608
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.893-842A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956608 | ||||||
| chr11:2956787
|
T | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(9): Show | 13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.893-1021A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956787 | ||||||
| chr11:2956822
|
G | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0013g0217 | 3 | HG02922.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.893-1056C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956822 | ||||||
| chr11:2956877
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.893-1111A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956877 | ||||||
| chr11:2956980
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(25): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.893-1214G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956980 | ||||||
| chr11:2956982
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893-1216A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956982 | ||||||
| chr11:2957076
|
T | TA | 9 | a0001c0001t0001g0214a0001c0002t0003g0014a0001c0002t0003g0111others(6): Show | 11 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.893-1311dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957076 | ||||||
| chr11:2957173
|
A | G | 10 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 10 | HG00099.hp2 HG01258.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+1226T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957173 | ||||||
| chr11:2957316
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0118others(10): Show | 14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.892+1083T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957316 | ||||||
| chr11:2957320
|
C | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(54): Show | 68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.892+1079G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957320 | ||||||
| chr11:2957479
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892+920C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957479 | ||||||
| chr11:2957481
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(10): Show | 19 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.892+918G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957481 | ||||||
| chr11:2957501
|
C | T | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.892+898G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957501 | ||||||
| chr11:2957542
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 12 | HG02083.hp1 NA18939.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.892+857A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957542 | ||||||
| chr11:2957630
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.892+769C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957630 | ||||||
| chr11:2957750
|
A | C | 1 | a0001c0001t0002g0085 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.892+649T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957750 | ||||||
| chr11:2957979
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.892+420G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957979 | ||||||
| chr11:2957999
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.892+400C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957999 | ||||||
| chr11:2958219
|
G | T | 1 | a0001c0001t0002g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.892+180C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958219 | ||||||
| chr11:2958229
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.892+170T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958229 | ||||||
| chr11:2958331
|
G | A | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+68C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958331 | ||||||
| chr11:2958557
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.747-13C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958557 | ||||||
| chr11:2958568
|
G | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.747-24C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958568 | ||||||
| chr11:2958715
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747-171C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958715 | ||||||
| chr11:2958891
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.747-347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958891 | ||||||
| chr11:2958989
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(9): Show | 13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-445T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958989 | ||||||
| chr11:2959006
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.747-462G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959006 | ||||||
| chr11:2959136
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.747-592A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959136 | ||||||
| chr11:2959150
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747-606G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959150 | ||||||
| chr11:2959201
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.746+569A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959201 | ||||||
| chr11:2959264
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.746+506A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959264 | ||||||
| chr11:2959393
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.746+377A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959393 | ||||||
| chr11:2959492
|
T | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.746+278A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959492 | ||||||
| chr11:2959601
|
T | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.746+169A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959601 | ||||||
| chr11:2959614
|
A | T | 1 | a0001c0002t0003g0014 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.746+156T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959614 | ||||||
| chr11:2959674
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.746+96G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959674 | ||||||
| chr11:2959939
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.607-30C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2959939 | ||||||
| chr11:2960055
|
A | G | 1 | a0001c0002t0003g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.607-146T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960055 | ||||||
| chr11:2960161
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.607-252C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960161 | ||||||
| chr11:2960164
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.607-255C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960164 | ||||||
| chr11:2960367
|
C | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(65): Show | 79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.607-458G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960367 | ||||||
| chr11:2960483
|
G | A | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-574C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960483 | ||||||
| chr11:2960486
|
A | C | 7 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(4): Show | 9 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-577T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960486 | ||||||
| chr11:2960552
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(28): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.607-643G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960552 | ||||||
| chr11:2960637
|
T | TG | 14 | a0001c0001t0001g0140a0001c0001t0001g0176a0001c0001t0001g0185others(11): Show | 14 | HG00438.hp2 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.607-729dupC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960637 | ||||||
| chr11:2960666
|
G | A | 114 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0153others(111): Show | 137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.607-757C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960666 | ||||||
| chr11:2960677
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0177 | 3 | HG00639.hp1 HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.607-768A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960677 | ||||||
| chr11:2960792
|
C | T | 5 | a0001c0001t0001g0257a0001c0001t0005g0027a0001c0001t0005g0278others(2): Show | 6 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-883G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960792 | ||||||
| chr11:2960851
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0181a0001c0001t0001g0182others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.607-942C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960851 | ||||||
| chr11:2960862
|
T | C | 84 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(81): Show | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.607-953A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960862 | ||||||
| chr11:2960921
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-1012T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960921 | ||||||
| chr11:2961022
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.607-1113T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961022 | ||||||
| chr11:2961110
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.607-1201A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961110 | ||||||
| chr11:2961125
|
C | CG | 159 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(156): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.607-1217dupC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961125 | ||||||
| chr11:2961125
|
C | CGG | 13 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0197others(10): Show | 19 | HG00639.hp2 HG01496.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.607-1218_607-1217d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961125 | ||||||
| chr11:2961217
|
C | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(68): Show | 87 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.607-1308G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961217 | ||||||
| chr11:2961233
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.607-1324C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961233 | ||||||
| chr11:2961253
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.607-1344A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961253 | ||||||
| chr11:2961343
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.607-1434G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961343 | ||||||
| chr11:2961361
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0182a0001c0001t0001g0191 | 4 | HG01109.hp1 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-1452T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961361 | ||||||
| chr11:2961497
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02723.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.607-1588C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961497 | ||||||
| chr11:2961501
|
T | TA | 79 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(76): Show | 99 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.607-1593dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961501 | ||||||
| chr11:2961501
|
TA | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 63 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.607-1593delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961501 | ||||||
| chr11:2962110
|
AACG | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(86): Show | 106 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.607-2204_607-2202d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962110 | ||||||
| chr11:2962170
|
C | T | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(200): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.607-2261G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962170 | ||||||
| chr11:2962171
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(29): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.607-2262G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962171 | ||||||
| chr11:2962241
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.607-2332T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962241 | ||||||
| chr11:2962264
|
G | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.607-2355C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962264 | ||||||
| chr11:2962523
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.606+2157G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962523 | ||||||
| chr11:2962545
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+2135C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962545 | ||||||
| chr11:2962557
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.606+2123A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962557 | ||||||
| chr11:2962563
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.606+2117T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962563 | ||||||
| chr11:2962707
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0082 | 2 | HG00280.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.606+1973T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962707 | ||||||
| chr11:2962756
|
G | A | 1 | a0001c0001t0014g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.606+1924C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962756 | ||||||
| chr11:2962937
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+1743A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962937 | ||||||
| chr11:2962960
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.606+1720G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962960 | ||||||
| chr11:2963074
|
T | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(76): Show | 91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.606+1606A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963074 | ||||||
| chr11:2963092
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0231 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.606+1588G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963092 | ||||||
| chr11:2963098
|
CA | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0018others(172): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.606+1581delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963098 | ||||||
| chr11:2963098
|
CAA | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(56): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.606+1580_606+1581d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963098 | ||||||
| chr11:2963105
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.606+1557_606+1574d others(20): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963105 | ||||||
| chr11:2963161
|
G | GA | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.606+1518dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963161 | ||||||
| chr11:2963172
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(8): Show | 12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1508C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963172 | ||||||
| chr11:2963228
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606+1452T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963228 | ||||||
| chr11:2963234
|
TACAAAGA others(6): Show |
T | 1 | a0001c0001t0002g0013 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.606+1433_606+1445d others(15): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963234 | ||||||
| chr11:2963399
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.606+1281A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963399 | ||||||
| chr11:2963414
|
G | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.606+1266C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963414 | ||||||
| chr11:2963415
|
C | G | 84 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(81): Show | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.606+1265G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963415 | ||||||
| chr11:2963440
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.606+1240C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963440 | ||||||
| chr11:2963485
|
G | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.606+1195C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963485 | ||||||
| chr11:2963579
|
C | A | 1 | a0001c0001t0002g0068 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.606+1101G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963579 | ||||||
| chr11:2963843
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(8): Show | 12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+837C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963843 | ||||||
| chr11:2963907
|
G | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.606+773C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963907 | ||||||
| chr11:2964123
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.606+557G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964123 | ||||||
| chr11:2964148
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.606+532T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964148 | ||||||
| chr11:2964176
|
G | C | 9 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(6): Show | 9 | NA18946.hp2 NA18948.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+504C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964176 | ||||||
| chr11:2964246
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0118others(10): Show | 14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+434C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964246 | ||||||
| chr11:2964311
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.606+369T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964311 | ||||||
| chr11:2964315
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.606+365G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964315 | ||||||
| chr11:2964632
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.606+48A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964632 | ||||||
| chr11:2964671
|
A | C | 1 | a0003c0007t0001g0119 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.606+9T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964671 | ||||||
| chr11:2964673
|
T | TA | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.606+6dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964673 | ||||||
| chr11:2964814
|
G | C | 3 | a0001c0004t0001g0023a0001c0004t0001g0235a0001c0004t0001g0253 | 4 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-63C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964814 | ||||||
| chr11:2964819
|
A | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-68T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964819 | ||||||
| chr11:2964926
|
G | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(65): Show | 79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.535-175C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964926 | ||||||
| chr11:2964955
|
C | T | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-204G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964955 | ||||||
| chr11:2965226
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.535-475T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965226 | ||||||
| chr11:2965470
|
C | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(65): Show | 79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.535-719G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965470 | ||||||
| chr11:2965546
|
A | G | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(94): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.535-795T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965546 | ||||||
| chr11:2965611
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535-860A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965611 | ||||||
| chr11:2965692
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(24): Show | 36 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.535-941C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965692 | ||||||
| chr11:2965760
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-1009C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965760 | ||||||
| chr11:2965776
|
C | A | 1 | a0001c0001t0002g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.535-1025G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965776 | ||||||
| chr11:2965823
|
C | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.535-1072G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965823 | ||||||
| chr11:2965859
|
C | A | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-1108G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965859 | ||||||
| chr11:2965867
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-1116C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965867 | ||||||
| chr11:2966005
|
C | T | 4 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1254G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966005 | ||||||
| chr11:2966013
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.535-1262C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966013 | ||||||
| chr11:2966056
|
A | G | 21 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-1305T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966056 | ||||||
| chr11:2966073
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.535-1322T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966073 | ||||||
| chr11:2966080
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535-1329A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966080 | ||||||
| chr11:2966088
|
T | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-1337A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966088 | ||||||
| chr11:2966191
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.535-1440A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966191 | ||||||
| chr11:2966413
|
T | TAACAGAC others(5): Show |
243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.535-1674_535-1663d others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966413 | ||||||
| chr11:2966649
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.535-1898C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966649 | ||||||
| chr11:2966798
|
A | G | 4 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0114others(1): Show | 6 | HG02451.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-2047T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966798 | ||||||
| chr11:2967009
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.535-2258T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967009 | ||||||
| chr11:2967093
|
C | T | 45 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0110others(42): Show | 47 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.535-2342G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967093 | ||||||
| chr11:2967138
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.535-2387C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967138 | ||||||
| chr11:2967201
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.535-2450A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967201 | ||||||
| chr11:2967357
|
A | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(53): Show | 67 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.534+2446T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967357 | ||||||
| chr11:2967369
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.534+2434A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967369 | ||||||
| chr11:2967391
|
T | C | 6 | a0001c0002t0003g0014a0001c0002t0003g0112a0001c0002t0003g0113others(3): Show | 8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+2412A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967391 | ||||||
| chr11:2967415
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0222others(8): Show | 15 | NA18942.hp1 NA18950.hp1 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.534+2388T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967415 | ||||||
| chr11:2967447
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(15): Show | 25 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.534+2356G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967447 | ||||||
| chr11:2967582
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.534+2221C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967582 | ||||||
| chr11:2967608
|
T | TA | 20 | a0001c0001t0001g0004a0001c0001t0001g0197a0001c0001t0001g0211others(17): Show | 27 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.534+2194dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967608 | ||||||
| chr11:2967616
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 12 | HG02083.hp1 NA18939.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.534+2187T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967616 | ||||||
| chr11:2967636
|
TA | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0139others(18): Show | 28 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+2166delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967636 | ||||||
| chr11:2967728
|
A | G | 1 | a0001c0005t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.534+2075T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967728 | ||||||
| chr11:2967817
|
C | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.534+1986G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967817 | ||||||
| chr11:2967912
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.534+1891T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967912 | ||||||
| chr11:2968202
|
A | G | 3 | a0002c0003t0001g0026a0002c0003t0001g0270a0002c0003t0001g0271 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1601T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968202 | ||||||
| chr11:2968219
|
G | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0197others(15): Show | 25 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.534+1584C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968219 | ||||||
| chr11:2968313
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.534+1490G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968313 | ||||||
| chr11:2968394
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.534+1409C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968394 | ||||||
| chr11:2968483
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.534+1320A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968483 | ||||||
| chr11:2968539
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+1264G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968539 | ||||||
| chr11:2968680
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01433.hp1 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1123G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968680 | ||||||
| chr11:2968770
|
G | A | 3 | a0001c0001t0002g0071a0001c0001t0002g0084a0001c0001t0002g0098 | 3 | HG01361.hp1 HG02055.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.534+1033C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968770 | ||||||
| chr11:2968806
|
G | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(209): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.534+997C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968806 | ||||||
| chr11:2968810
|
A | G | 3 | a0001c0002t0003g0112a0001c0002t0003g0113a0001c0002t0003g0115 | 3 | HG01884.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.534+993T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968810 | ||||||
| chr11:2968820
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.534+983A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968820 | ||||||
| chr11:2968914
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(95): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.534+889G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968914 | ||||||
| chr11:2968953
|
AATCAGAA others(7): Show |
A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+836_534+849del others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968953 | ||||||
| chr11:2968985
|
G | A | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.534+818C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968985 | ||||||
| chr11:2968988
|
G | GT | 17 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(14): Show | 19 | HG00423.hp1 HG00642.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.534+814dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968988 | ||||||
| chr11:2968988
|
GT | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.534+814delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968988 | ||||||
| chr11:2968994
|
T | TG | 80 | a0001c0001t0001g0044a0001c0001t0001g0159a0001c0001t0002g0001others(77): Show | 101 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.534+808_534+809ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968994 | ||||||
| chr11:2968995
|
T | G | 31 | a0001c0001t0001g0018a0001c0001t0001g0153a0001c0001t0001g0179others(28): Show | 33 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.534+808A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968995 | ||||||
| chr11:2968996
|
T | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.534+807A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968996 | ||||||
| chr11:2968997
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534+806A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968997 | ||||||
| chr11:2969023
|
C | CT | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.534+779_534+780ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969023 | ||||||
| chr11:2969148
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+655C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969148 | ||||||
| chr11:2969188
|
G | A | 2 | a0001c0001t0004g0154a0001c0001t0004g0157 | 2 | HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.534+615C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969188 | ||||||
| chr11:2969215
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0171 | 2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.534+588C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969215 | ||||||
| chr11:2969296
|
G | A | 85 | a0001c0001t0001g0044a0001c0001t0001g0159a0001c0001t0002g0001others(82): Show | 105 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.534+507C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969296 | ||||||
| chr11:2969316
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.534+487C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969316 | ||||||
| chr11:2969365
|
T | TAC | 2 | a0001c0001t0001g0153a0001c0002t0007g0015 | 3 | HG01433.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.534+436_534+437dup others(2): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969365 | ||||||
| chr11:2969365
|
T | TACAC | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+434_534+437dup others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969365 | ||||||
| chr11:2969463
|
G | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.534+340C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969463 | ||||||
| chr11:2969483
|
G | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(95): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.534+320C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969483 | ||||||
| chr11:2969545
|
T | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.534+258A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969545 | ||||||
| chr11:2969582
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.534+221A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969582 | ||||||
| chr11:2969622
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(25): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.534+181A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969622 | ||||||
| chr11:2969755
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.534+48C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969755 | ||||||
| chr11:2969790
|
G | A | 2 | a0001c0001t0002g0040a0001c0001t0002g0086 | 2 | NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.534+13C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969790 | ||||||
| chr11:2969989
|
C | G | 94 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0001g0159others(91): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.403-55G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2969989 | ||||||
| chr11:2970160
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.403-226T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970160 | ||||||
| chr11:2970240
|
C | T | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.403-306G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970240 | ||||||
| chr11:2970280
|
A | G | 1 | a0001c0001t0004g0154 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403-346T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970280 | ||||||
| chr11:2970301
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0006t0001g0240 | 3 | HG00438.hp1 HG00558.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.403-367C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970301 | ||||||
| chr11:2970333
|
T | C | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.403-399A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970333 | ||||||
| chr11:2970438
|
A | T | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(207): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.403-504T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970438 | ||||||
| chr11:2970443
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.403-509G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970443 | ||||||
| chr11:2970662
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.403-728C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970662 | ||||||
| chr11:2970848
|
AC | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.402+599delG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970848 | ||||||
| chr11:2970848
|
ACCC | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(52): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.402+597_402+599del others(3): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970848 | ||||||
| chr11:2970856
|
CCCA | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(65): Show | 80 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.402+589_402+591del others(3): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970856 | ||||||
| chr11:2970857
|
C | A | 5 | a0001c0001t0002g0034a0001c0001t0002g0045a0001c0001t0002g0047others(2): Show | 5 | NA18964.hp1 NA19002.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+591G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970857 | ||||||
| chr11:2970857
|
C | CA | 74 | a0001c0001t0001g0044a0001c0001t0001g0159a0001c0001t0002g0001others(71): Show | 94 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.402+590_402+591ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970857 | ||||||
| chr11:2970858
|
C | A | 81 | a0001c0001t0001g0044a0001c0001t0001g0159a0001c0001t0002g0001others(78): Show | 101 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.402+590G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970858 | ||||||
| chr11:2970858
|
C | CA | 9 | a0001c0001t0001g0153a0001c0001t0002g0031a0001c0002t0003g0014others(6): Show | 11 | HG01433.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+589dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970858 | ||||||
| chr11:2970887
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.402+561T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970887 | ||||||
| chr11:2970888
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.402+560C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970888 | ||||||
| chr11:2970923
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.402+525C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970923 | ||||||
| chr11:2970930
|
A | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.402+518T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970930 | ||||||
| chr11:2971124
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(28): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.402+324T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2971124 | ||||||
| chr11:2971297
|
A | G | 1 | a0001c0001t0014g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.402+151T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2971297 | ||||||
| chr11:2971841
|
CCTCT | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(29): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.315+257_315+260del others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/15 | chr11 | 2971841 | ||||||
| chr11:2971967
|
G | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(88): Show | 108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.315+135C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/15 | chr11 | 2971967 | ||||||
| chr11:2972502
|
G | C | 1 | a0001c0001t0010g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.174-259C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972502 | ||||||
| chr11:2972543
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.174-300A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972543 | ||||||
| chr11:2972644
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.174-401T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972644 | ||||||
| chr11:2972697
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0073 | 2 | NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.174-454G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972697 | ||||||
| chr11:2972707
|
C | T | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.174-464G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972707 | ||||||
| chr11:2972827
|
A | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(216): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.174-584T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972827 | ||||||
| chr11:2972898
|
G | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(88): Show | 108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.174-655C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972898 | ||||||
| chr11:2972928
|
G | C | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.174-685C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972928 | ||||||
| chr11:2972962
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.174-719G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972962 | ||||||
| chr11:2972991
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174-748A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972991 | ||||||
| chr11:2972991
|
T | C | 1 | a0001c0001t0004g0156 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174-748A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972991 | ||||||
| chr11:2973271
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.174-1028T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973271 | ||||||
| chr11:2973681
|
T | C | 1 | a0001c0002t0003g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174-1438A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973681 | ||||||
| chr11:2973711
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.174-1468C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973711 | ||||||
| chr11:2973748
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.174-1505T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973748 | ||||||
| chr11:2973832
|
G | A | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.174-1589C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973832 | ||||||
| chr11:2973837
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.174-1594G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973837 | ||||||
| chr11:2973917
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.174-1674T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973917 | ||||||
| chr11:2973955
|
T | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174-1712A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973955 | ||||||
| chr11:2973956
|
A | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174-1713T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973956 | ||||||
| chr11:2974022
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.174-1779G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974022 | ||||||
| chr11:2974085
|
T | A | 3 | a0002c0003t0001g0026a0002c0003t0001g0270a0002c0003t0001g0271 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-1842A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974085 | ||||||
| chr11:2974111
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.174-1868G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974111 | ||||||
| chr11:2974237
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.173+1787G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974237 | ||||||
| chr11:2974238
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.173+1786C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974238 | ||||||
| chr11:2974546
|
C | T | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+1478G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974546 | ||||||
| chr11:2974654
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.173+1370C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974654 | ||||||
| chr11:2974659
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.173+1365C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974659 | ||||||
| chr11:2974742
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173+1272_173+1281d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974742 | ||||||
| chr11:2974884
|
T | C | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.173+1140A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974884 | ||||||
| chr11:2974969
|
A | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(31): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.173+1055T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974969 | ||||||
| chr11:2975049
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01081.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.173+975G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975049 | ||||||
| chr11:2975106
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.173+918C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975106 | ||||||
| chr11:2975152
|
T | A | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.173+872A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | ||||||
| chr11:2975152
|
T | TA | 31 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(28): Show | 34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.173+871dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | ||||||
| chr11:2975152
|
T | TAA | 86 | a0001c0001t0001g0044a0001c0001t0001g0118a0001c0001t0001g0147others(83): Show | 106 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.173+870_173+871dup others(2): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | ||||||
| chr11:2975152
|
TA | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0162others(20): Show | 29 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.173+871delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | ||||||
| chr11:2975245
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 7 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+779C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975245 | ||||||
| chr11:2975302
|
G | A | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | NA18946.hp2 NA18955.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+722C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975302 | ||||||
| chr11:2975392
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+632A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975392 | ||||||
| chr11:2975459
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.173+565T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975459 | ||||||
| chr11:2975479
|
C | T | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.173+545G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975479 | ||||||
| chr11:2975557
|
C | T | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.173+467G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975557 | ||||||
| chr11:2975817
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.173+207C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975817 | ||||||
| chr11:2975856
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.173+168C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975856 | ||||||
| chr11:2975859
|
C | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+165G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975859 | ||||||
| chr11:2975902
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.173+122A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975902 | ||||||
| chr11:2976156
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.74-33A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976156 | ||||||
| chr11:2976255
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.74-132C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976255 | ||||||
| chr11:2976374
|
GCTCTCAC others(5): Show |
G | 1 | a0001c0001t0002g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74-263_74-252delTC others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976374 | ||||||
| chr11:2976456
|
C | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.74-333G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976456 | ||||||
| chr11:2976457
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74-334G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976457 | ||||||
| chr11:2976468
|
G | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(25): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.74-345C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976468 | ||||||
| chr11:2976616
|
G | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.74-493C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976616 | ||||||
| chr11:2976623
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0197a0001c0001t0001g0211others(9): Show | 18 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.74-500A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976623 | ||||||
| chr11:2976716
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.74-593G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976716 | ||||||
| chr11:2976920
|
C | T | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74-797G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976920 | ||||||
| chr11:2976946
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(66): Show | 81 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.74-823G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976946 | ||||||
| chr11:2976949
|
ACCCGAGT others(10): Show |
A | 3 | a0001c0001t0001g0197a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG02647.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.74-843_74-827delAT others(15): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976949 | ||||||
| chr11:2976969
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.74-846G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976969 | ||||||
| chr11:2976984
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.74-861G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976984 | ||||||
| chr11:2977049
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.74-926G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977049 | ||||||
| chr11:2977132
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74-1009A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977132 | ||||||
| chr11:2977152
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0199 | 3 | HG02109.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.74-1029T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977152 | ||||||
| chr11:2977194
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-1071G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977194 | ||||||
| chr11:2977231
|
C | T | 84 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(81): Show | 104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.73+1053G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977231 | ||||||
| chr11:2977237
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+1047C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977237 | ||||||
| chr11:2977324
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.73+960A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977324 | ||||||
| chr11:2977392
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 7 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+892C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977392 | ||||||
| chr11:2977640
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(77): Show | 92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.73+644T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977640 | ||||||
| chr11:2977679
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+605T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977679 | ||||||
| chr11:2977682
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | HG01346.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+602C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977682 | ||||||
| chr11:2977703
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0197a0001c0001t0001g0211others(12): Show | 22 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.73+581C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977703 | ||||||
| chr11:2977708
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.73+576A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977708 | ||||||
| chr11:2977718
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.73+566G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977718 | ||||||
| chr11:2977762
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73+522A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977762 | ||||||
| chr11:2977772
|
T | A | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.73+512A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977772 | ||||||
| chr11:2977788
|
T | C | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73+496A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977788 | ||||||
| chr11:2977866
|
T | TA | 82 | a0001c0001t0001g0044a0001c0001t0001g0194a0001c0001t0001g0195others(79): Show | 102 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.73+417dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | ||||||
| chr11:2977866
|
TA | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(88): Show | 109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.73+417delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | ||||||
| chr11:2977866
|
TAA | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 6 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+416_73+417delTT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | ||||||
| chr11:2977914
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.73+370G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977914 | ||||||
| chr11:2978019
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+265A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978019 | ||||||
| chr11:2978049
|
C | G | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(94): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.73+235G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978049 | ||||||
| chr11:2978257
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73+27G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978257 | ||||||
| chr11:2978277
|
G | T | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
splice_region_variant&intron_variant | LOW | c.73+7C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978277 | ||||||
| chr11:2978355
|
T | A | 9 | a0001c0001t0001g0257a0001c0001t0002g0258a0001c0001t0005g0027others(6): Show | 11 | HG00642.hp1 HG01243.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15-13A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978355 | ||||||
| chr11:2978370
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-28A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978370 | ||||||
| chr11:2978371
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.15-29A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978371 | ||||||
| chr11:2978418
|
T | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-76A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978418 | ||||||
| chr11:2978441
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.15-99A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978441 | ||||||
| chr11:2978683
|
G | C | 1 | a0001c0001t0006g0275 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15-341C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978683 | ||||||
| chr11:2978689
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(31): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.15-347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978689 | ||||||
| chr11:2978907
|
C | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(29): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.14+300G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978907 | ||||||
| chr11:2978949
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.14+258T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978949 | ||||||
| chr11:2978968
|
T | TA | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.14+238dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978968 | ||||||
| chr11:2979056
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.14+151A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979056 | ||||||
| chr11:2979100
|
G | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.14+107C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979100 | ||||||
| chr11:2979165
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.14+42G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979165 | ||||||
| chr11:2979254
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-17C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979254 | ||||||
| chr11:2979299
|
T | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-62A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979299 | ||||||
| chr11:2979339
|
A | C | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-17-102T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979339 | ||||||
| chr11:2979512
|
C | T | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-275G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979512 | ||||||
| chr11:2979526
|
A | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-17-289T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979526 | ||||||
| chr11:2979528
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-291A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979528 | ||||||
| chr11:2979771
|
T | TA | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 105 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-17-535dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979771 | ||||||
| chr11:2979778
|
A | AT | 14 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0197others(11): Show | 15 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-542_-17-541ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979778 | ||||||
| chr11:2979783
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-546A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979783 | ||||||
| chr11:2979870
|
C | T | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 9 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-633G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979870 | ||||||
| chr11:2979875
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-17-638C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979875 | ||||||
| chr11:2979890
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-17-653G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979890 | ||||||
| chr11:2980164
|
A | G | 1 | a0001c0001t0006g0276 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-17-927T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980164 | ||||||
| chr11:2980383
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-1146G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980383 | ||||||
| chr11:2980477
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-17-1240G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980477 | ||||||
| chr11:2980477
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-1240G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980477 | ||||||
| chr11:2980478
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-17-1241C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980478 | ||||||
| chr11:2980584
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-1347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980584 | ||||||
| chr11:2980621
|
G | T | 1 | a0001c0001t0011g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-1384C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980621 | ||||||
| chr11:2980777
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-1540T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980777 | ||||||
| chr11:2980837
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(31): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.-17-1600G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980837 | ||||||
| chr11:2980934
|
G | GA | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-1698dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980934 | ||||||
| chr11:2980934
|
GA | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-1698delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980934 | ||||||
| chr11:2980957
|
A | AGT | 6 | a0001c0002t0003g0014a0001c0002t0003g0112a0001c0002t0003g0113others(3): Show | 8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-1722_-17-1721d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980957 | ||||||
| chr11:2980997
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-1760T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980997 | ||||||
| chr11:2981058
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-17-1821G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981058 | ||||||
| chr11:2981068
|
AAAAC | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-1835_-17-1832d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981068 | ||||||
| chr11:2981102
|
C | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-17-1865G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981102 | ||||||
| chr11:2981246
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-2009C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981246 | ||||||
| chr11:2981246
|
G | GA | 76 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(73): Show | 88 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-17-2010dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981246 | ||||||
| chr11:2981248
|
A | T | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-2011T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981248 | ||||||
| chr11:2981278
|
C | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(206): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-17-2041G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981278 | ||||||
| chr11:2981364
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-2127G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981364 | ||||||
| chr11:2981368
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-2131A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981368 | ||||||
| chr11:2981369
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-2132C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981369 | ||||||
| chr11:2981373
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0247others(2): Show | 10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-2136C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981373 | ||||||
| chr11:2981374
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-2137G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981374 | ||||||
| chr11:2981417
|
T | TC | 12 | a0001c0001t0001g0024a0001c0001t0001g0141a0001c0001t0001g0233others(9): Show | 13 | HG02056.hp2 HG02738.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-2181dupG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981417 | ||||||
| chr11:2981418
|
C | CA | 10 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0137others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2182dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
C | CAAAAAA | 9 | a0001c0001t0002g0006a0001c0001t0002g0046a0001c0001t0002g0047others(6): Show | 11 | HG01071.hp1 HG01993.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-2187_-17-2182d others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
C | CAAAAAAA | 27 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0012others(24): Show | 35 | HG00438.hp2 HG01081.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.-17-2188_-17-2182d others(9): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
C | CAAAAAAA others(1): Show |
26 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0035others(23): Show | 36 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-2189_-17-2182d others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0044a0001c0001t0002g0043a0001c0001t0002g0074others(11): Show | 14 | HG00621.hp1 HG00735.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-2190_-17-2182d others(11): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0082others(4): Show | 7 | HG00280.hp2 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-2191_-17-2182d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
CA | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0019others(46): Show | 60 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.-17-2182delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
CAA | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0197a0001c0001t0001g0210others(3): Show | 7 | HG01243.hp1 HG01516.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-2183_-17-2182d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
CAAAAAAA | C | 9 | a0001c0001t0001g0118a0001c0001t0001g0147a0001c0001t0001g0180others(6): Show | 9 | HG00099.hp2 HG01258.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-2188_-17-2182d others(9): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0181others(10): Show | 14 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-2189_-17-2182d others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981418
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0010g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-2193_-17-2182d others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | ||||||
| chr11:2981419
|
A | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(41): Show | 54 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-17-2182T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981419 | ||||||
| chr11:2981420
|
A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0028others(31): Show | 41 | HG00639.hp2 HG01346.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.-17-2183T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981420 | ||||||
| chr11:2981421
|
A | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0210a0002c0003t0001g0026others(2): Show | 6 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2184T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981421 | ||||||
| chr11:2981431
|
A | C | 1 | a0001c0001t0010g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-2194T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981431 | ||||||
| chr11:2981571
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(76): Show | 91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-17-2334C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981571 | ||||||
| chr11:2981587
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-2350G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981587 | ||||||
| chr11:2981610
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-2373G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981610 | ||||||
| chr11:2981688
|
A | G | 93 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0002g0001others(90): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-17-2451T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981688 | ||||||
| chr11:2981699
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-17-2462G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981699 | ||||||
| chr11:2981735
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17-2498C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981735 | ||||||
| chr11:2981823
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-2586C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981823 | ||||||
| chr11:2981861
|
G | A | 4 | a0001c0001t0002g0258a0002c0003t0001g0026a0002c0003t0001g0270others(1): Show | 5 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-2624C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981861 | ||||||
| chr11:2981870
|
T | A | 1 | a0001c0005t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-2633A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981870 | ||||||
| chr11:2981912
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-2675G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981912 | ||||||
| chr11:2982026
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0086 | 2 | NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-17-2789T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982026 | ||||||
| chr11:2982107
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-17-2870T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982107 | ||||||
| chr11:2982170
|
C | T | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2933G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982170 | ||||||
| chr11:2982172
|
T | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2935A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982172 | ||||||
| chr11:2982256
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-17-3019G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982256 | ||||||
| chr11:2982432
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0136a0001c0001t0001g0138 | 5 | HG01099.hp1 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-3195A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982432 | ||||||
| chr11:2982571
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-3334G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982571 | ||||||
| chr11:2982589
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-17-3352G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982589 | ||||||
| chr11:2982716
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-17-3479G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982716 | ||||||
| chr11:2982775
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-3538G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982775 | ||||||
| chr11:2983035
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-3798T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983035 | ||||||
| chr11:2983211
|
A | T | 1 | a0002c0003t0001g0270 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-3974T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983211 | ||||||
| chr11:2983296
|
C | G | 85 | a0001c0001t0001g0044a0001c0001t0001g0150a0001c0001t0001g0153others(82): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-17-4059G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983296 | ||||||
| chr11:2983388
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-17-4151C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983388 | ||||||
| chr11:2983550
|
A | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(70): Show | 85 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-17-4313T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983550 | ||||||
| chr11:2983583
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-17-4346C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983583 | ||||||
| chr11:2983592
|
G | GA | 125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-17-4356dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983592 | ||||||
| chr11:2983592
|
GA | G | 9 | a0001c0001t0001g0159a0001c0001t0006g0274a0001c0002t0003g0014others(6): Show | 11 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-4356delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983592 | ||||||
| chr11:2983611
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-4374T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983611 | ||||||
| chr11:2983695
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-17-4458T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983695 | ||||||
| chr11:2983750
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(95): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-4513T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983750 | ||||||
| chr11:2983796
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-4559G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983796 | ||||||
| chr11:2983804
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-4567T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983804 | ||||||
| chr11:2983891
|
C | CAGG | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(95): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-4657_-17-4655d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983891 | ||||||
| chr11:2983923
|
T | C | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-4686A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983923 | ||||||
| chr11:2983957
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-4720C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983957 | ||||||
| chr11:2983994
|
GA | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(140): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-17-4758delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983994 | ||||||
| chr11:2984042
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17-4805G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984042 | ||||||
| chr11:2984096
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-17-4859G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984096 | ||||||
| chr11:2984121
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-17-4884A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984121 | ||||||
| chr11:2984124
|
G | A | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-4887C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984124 | ||||||
| chr11:2984166
|
C | CA | 31 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0029others(28): Show | 33 | HG00438.hp1 HG00558.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-4930dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | ||||||
| chr11:2984166
|
CA | C | 15 | a0001c0001t0001g0118a0001c0001t0001g0153a0001c0001t0001g0175others(12): Show | 16 | HG00642.hp1 HG01433.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-4930delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | ||||||
| chr11:2984166
|
CAA | C | 35 | a0001c0001t0001g0018a0001c0001t0001g0132a0001c0001t0001g0149others(32): Show | 38 | HG00099.hp2 HG01109.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-4931_-17-4930d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | ||||||
| chr11:2984166
|
CAAA | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(103): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-17-4932_-17-4930d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | ||||||
| chr11:2984190
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-17-4953C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984190 | ||||||
| chr11:2984236
|
A | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0002g0043 | 3 | HG00733.hp1 HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-17-4999T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984236 | ||||||
| chr11:2984287
|
CA | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-5051delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984287 | ||||||
| chr11:2984349
|
G | A | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-5112C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984349 | ||||||
| chr11:2984440
|
G | A | 98 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0001g0140others(95): Show | 120 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-17-5203C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984440 | ||||||
| chr11:2984513
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-5276C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984513 | ||||||
| chr11:2984692
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0136a0001c0001t0001g0138 | 5 | HG01099.hp1 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-5455C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984692 | ||||||
| chr11:2984797
|
ACAG | A | 89 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0001g0140others(86): Show | 109 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-17-5563_-17-5561d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984797 | ||||||
| chr11:2984870
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-17-5633G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984870 | ||||||
| chr11:2985397
|
ATC | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(63): Show | 78 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-6162_-17-6161d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985397 | ||||||
| chr11:2985417
|
A | T | 1 | a0001c0002t0003g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-6180T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985417 | ||||||
| chr11:2985434
|
A | AGTCTTAT others(30): Show |
1 | a0001c0001t0001g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-17-6234_-17-6198d others(39): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985434 | ||||||
| chr11:2985703
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-17-6466A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985703 | ||||||
| chr11:2985719
|
ACAAT | A | 6 | a0001c0002t0003g0014a0001c0002t0003g0112a0001c0002t0003g0113others(3): Show | 8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-6486_-17-6483d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985719 | ||||||
| chr11:2985752
|
CA | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(62): Show | 77 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-18+6501delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985752 | ||||||
| chr11:2985863
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+6391A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985863 | ||||||
| chr11:2985905
|
A | G | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+6349T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985905 | ||||||
| chr11:2985914
|
CT | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+6339delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985914 | ||||||
| chr11:2986252
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-18+6002T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986252 | ||||||
| chr11:2986263
|
A | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18+5991T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986263 | ||||||
| chr11:2986311
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+5943A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986311 | ||||||
| chr11:2986318
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+5936C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986318 | ||||||
| chr11:2986344
|
A | C | 1 | a0001c0001t0002g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18+5910T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986344 | ||||||
| chr11:2986352
|
C | T | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+5902G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986352 | ||||||
| chr11:2986355
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+5899G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986355 | ||||||
| chr11:2986372
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-18+5882A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986372 | ||||||
| chr11:2986373
|
C | CA | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+5880dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986373 | ||||||
| chr11:2986373
|
CA | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(73): Show | 93 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18+5880delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986373 | ||||||
| chr11:2986377
|
AAAAAAAA others(4): Show |
A | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 9 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+5866_-18+5876d others(13): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986377 | ||||||
| chr11:2986382
|
AAAAAAG | A | 95 | a0001c0001t0001g0044a0001c0001t0001g0140a0001c0001t0001g0141others(92): Show | 117 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-18+5866_-18+5871d others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986382 | ||||||
| chr11:2986383
|
AAAAAGAA others(4): Show |
A | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+5860_-18+5870d others(13): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986383 | ||||||
| chr11:2986417
|
C | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-18+5837G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986417 | ||||||
| chr11:2986468
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+5786T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986468 | ||||||
| chr11:2986592
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18+5662G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986592 | ||||||
| chr11:2986626
|
A | AT | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-18+5627dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | ||||||
| chr11:2986626
|
A | ATT | 11 | a0001c0001t0001g0123a0001c0001t0001g0251a0001c0001t0002g0039others(8): Show | 13 | HG01884.hp1 HG02056.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18+5626_-18+5627d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | ||||||
| chr11:2986626
|
A | ATTTT | 17 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(14): Show | 18 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+5624_-18+5627d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | ||||||
| chr11:2986626
|
A | T | 1 | a0001c0001t0002g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+5628T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | ||||||
| chr11:2986656
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18+5598G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986656 | ||||||
| chr11:2986661
|
T | G | 4 | a0001c0001t0005g0027a0001c0001t0005g0278a0001c0001t0005g0279others(1): Show | 5 | HG00642.hp1 HG02258.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+5593A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986661 | ||||||
| chr11:2986696
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0020others(48): Show | 62 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-18+5558C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986696 | ||||||
| chr11:2986784
|
AT | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-18+5469delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986784 | ||||||
| chr11:2986920
|
C | CACCCAG | 240 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-18+5333_-18+5334i others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986920 | ||||||
| chr11:2987099
|
C | T | 1 | a0001c0001t0006g0274 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-18+5155G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987099 | ||||||
| chr11:2987174
|
G | A | 89 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0001g0140others(86): Show | 109 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-18+5080C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987174 | ||||||
| chr11:2987199
|
T | TGCCCAGG others(3): Show |
1 | a0001c0001t0001g0175 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-18+5045_-18+5054d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987199 | ||||||
| chr11:2987280
|
A | G | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+4974T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987280 | ||||||
| chr11:2987464
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-18+4790C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987464 | ||||||
| chr11:2987502
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02723.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+4752A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987502 | ||||||
| chr11:2987662
|
CAGG | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0197a0001c0001t0001g0211others(9): Show | 18 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+4589_-18+4591d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987662 | ||||||
| chr11:2987700
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-18+4554A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987700 | ||||||
| chr11:2987712
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+4542C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987712 | ||||||
| chr11:2987744
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18+4510C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987744 | ||||||
| chr11:2987753
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(110): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18+4501G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987753 | ||||||
| chr11:2987756
|
C | CA | 16 | a0001c0001t0001g0138a0001c0001t0001g0147a0001c0001t0001g0149others(13): Show | 16 | HG00140.hp2 HG01109.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+4497dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | ||||||
| chr11:2987756
|
C | CAAA | 16 | a0001c0001t0001g0018a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 17 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+4495_-18+4497d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | ||||||
| chr11:2987756
|
CA | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0044others(103): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-18+4497delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | ||||||
| chr11:2987756
|
CAA | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0001g0121others(3): Show | 7 | HG01168.hp1 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+4496_-18+4497d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | ||||||
| chr11:2987794
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+4460C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987794 | ||||||
| chr11:2987907
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+4347A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987907 | ||||||
| chr11:2987982
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+4272A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987982 | ||||||
| chr11:2987990
|
C | T | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+4264G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987990 | ||||||
| chr11:2988040
|
A | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-18+4214T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988040 | ||||||
| chr11:2988116
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(22): Show | 34 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+4138C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988116 | ||||||
| chr11:2988134
|
T | C | 6 | a0001c0001t0001g0257a0001c0001t0002g0258a0001c0001t0005g0027others(3): Show | 7 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+4120A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988134 | ||||||
| chr11:2988161
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-18+4093G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988161 | ||||||
| chr11:2988197
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(25): Show | 38 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.-18+4057C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988197 | ||||||
| chr11:2988203
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18+4051C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988203 | ||||||
| chr11:2988208
|
T | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(110): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18+4046A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988208 | ||||||
| chr11:2988311
|
GTCATCTT others(30): Show |
G | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+3906_-18+3942d others(39): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988311 | ||||||
| chr11:2988330
|
A | C | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3924T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988330 | ||||||
| chr11:2988351
|
A | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+3903T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988351 | ||||||
| chr11:2988410
|
A | G | 91 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0001g0140others(88): Show | 111 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-18+3844T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988410 | ||||||
| chr11:2988540
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18+3714T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988540 | ||||||
| chr11:2988579
|
G | C | 1 | a0001c0001t0009g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+3675C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988579 | ||||||
| chr11:2988691
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-18+3563T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988691 | ||||||
| chr11:2988819
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-18+3435A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988819 | ||||||
| chr11:2988824
|
A | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(88): Show | 109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+3430T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988824 | ||||||
| chr11:2988854
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3400G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988854 | ||||||
| chr11:2988862
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3392T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988862 | ||||||
| chr11:2988868
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+3386A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988868 | ||||||
| chr11:2988998
|
T | A | 1 | a0001c0001t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-18+3256A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988998 | ||||||
| chr11:2989083
|
A | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0110a0001c0001t0001g0199others(10): Show | 14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+3171T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989083 | ||||||
| chr11:2989160
|
C | T | 92 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0001g0140others(89): Show | 112 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-18+3094G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989160 | ||||||
| chr11:2989200
|
A | G | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+3054T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989200 | ||||||
| chr11:2989273
|
T | G | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+2981A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989273 | ||||||
| chr11:2989276
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18+2978T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989276 | ||||||
| chr11:2989410
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-18+2844G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989410 | ||||||
| chr11:2989573
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+2681T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989573 | ||||||
| chr11:2989581
|
CTA | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | NA18952.hp2 NA18955.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2671_-18+2672d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989581 | ||||||
| chr11:2989594
|
C | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(87): Show | 108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+2660G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989594 | ||||||
| chr11:2989611
|
C | G | 9 | a0001c0001t0009g0198a0001c0002t0003g0014a0001c0002t0003g0111others(6): Show | 11 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+2643G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989611 | ||||||
| chr11:2989631
|
T | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0179a0001c0001t0001g0180others(17): Show | 21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+2623A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989631 | ||||||
| chr11:2989756
|
G | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(94): Show | 115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-18+2498C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989756 | ||||||
| chr11:2989873
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+2381C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989873 | ||||||
| chr11:2989958
|
CAT | C | 3 | a0002c0003t0001g0026a0002c0003t0001g0270a0002c0003t0001g0271 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2294_-18+2295d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989958 | ||||||
| chr11:2990043
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18+2211T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990043 | ||||||
| chr11:2990114
|
AT | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18+2139delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990114 | ||||||
| chr11:2990121
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(26): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18+2133T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990121 | ||||||
| chr11:2990129
|
AT | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2124delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990129 | ||||||
| chr11:2990132
|
T | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2122A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990132 | ||||||
| chr11:2990133
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2121C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990133 | ||||||
| chr11:2990135
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2119C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990135 | ||||||
| chr11:2990136
|
CCTA | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2115_-18+2117d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990136 | ||||||
| chr11:2990138
|
T | G | 3 | a0002c0003t0001g0026a0002c0003t0001g0270a0002c0003t0001g0271 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2116A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990138 | ||||||
| chr11:2990149
|
T | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(89): Show | 110 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-18+2105A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990149 | ||||||
| chr11:2990245
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0011g0117 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-18+2009C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990245 | ||||||
| chr11:2990291
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18+1963G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990291 | ||||||
| chr11:2990636
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-18+1618G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990636 | ||||||
| chr11:2990819
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-18+1435C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990819 | ||||||
| chr11:2990841
|
A | T | 1 | a0001c0002t0015g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+1413T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990841 | ||||||
| chr11:2990892
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+1362T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990892 | ||||||
| chr11:2990909
|
C | G | 8 | a0001c0002t0003g0014a0001c0002t0003g0111a0001c0002t0003g0112others(5): Show | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+1345G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990909 | ||||||
| chr11:2990956
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+1298T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990956 | ||||||
| chr11:2990994
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-18+1260A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990994 | ||||||
| chr11:2991331
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+923A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991331 | ||||||
| chr11:2991411
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+843A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991411 | ||||||
| chr11:2991439
|
A | AT | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+814dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991439 | ||||||
| chr11:2991674
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0031 | 3 | NA18939.hp1 NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-18+580T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991674 | ||||||
| chr11:2991928
|
G | A | 1 | a0001c0001t0002g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+326C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991928 | ||||||
| chr11:2992057
|
C | G | 83 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0003others(80): Show | 103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-18+197G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992057 | ||||||
| chr11:2992084
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18+170C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992084 | ||||||
| chr11:2992086
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-18+168G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992086 | ||||||
| chr11:2992098
|
C | G | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0272others(3): Show | 7 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+156G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992098 | ||||||
| chr11:2992162
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0272others(3): Show | 7 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+92C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992162 | ||||||
| chr11:2992177
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18+77C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992177 |