Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4799 |
|---|---|
| ensemblid | ENSG00000086102.19 |
| hgncid | 7803 |
| symbol | NFX1 |
| name | nuclear transcription factor, X-box binding 1 |
| refseq_nuc | NM_002504.6 |
| refseq_prot | NP_002495.2 |
| ensembl_nuc | ENST00000379540.8 |
| ensembl_prot | ENSP00000368856.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 33290516 |
| end | 33371157 |
| strand | + |
| ver | v1.2 |
| region | chr9:33290516-33371157 |
| region5000 | chr9:33285516-33376157 |
| regionname0 | NFX1_chr9_33290516_33371157 |
| regionname5000 | NFX1_chr9_33285516_33376157 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1120 | 282 | 72 | 50 | 128 | 10 | 20 | 98 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002 | 0/0 | 1120 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0003 | 0/0 | 1120 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0004 | 0/0 | 1120 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0005 | 0/0 | 1120 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0006 | 0/0 | 1120 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0007 | 0/0 | 1120 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3363 | 270 | 66 | 48 | 127 | 10 | 17 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0002 | 0/0 | 3363 | 8 | 6 | 2 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0003 | 0/0 | 3363 | 6 | 6 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0004 | 0/0 | 3363 | 4 | 0 | 0 | 4 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0005 | 0/0 | 3363 | 3 | 0 | 0 | 0 | 0 | 3 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0006 | 0/0 | 3363 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0007 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0008 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0009 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0010 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0011 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0012 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| c0013 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1237 | 214 | 58 | 32 | 99 | 9 | 15 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0002 | 1/0 | 1237 | 75 | 14 | 17 | 37 | 1 | 5 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0003 | 0/0 | 1237 | 6 | 5 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0004 | 0/0 | 1237 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0005 | 0/0 | 1237 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0006 | 0/0 | 1237 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| t0007 | 0/0 | 1237 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3363 | 270 | 66 | 48 | 127 | 10 | 17 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0003 | 0/0 | 3363 | 6 | 6 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0005 | 0/0 | 3363 | 3 | 0 | 0 | 0 | 0 | 3 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0008 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0010 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0012 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002c0002 | 0/0 | 3363 | 8 | 6 | 2 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002c0006 | 0/0 | 3363 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0003c0004 | 0/0 | 3363 | 4 | 0 | 0 | 4 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0004c0011 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0005c0009 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0006c0007 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0007c0013 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4599 | 195 | 49 | 30 | 91 | 9 | 15 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0001t0002 | 1/0 | 4599 | 70 | 14 | 16 | 36 | 1 | 2 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0001t0004 | 0/0 | 4599 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0001t0005 | 0/0 | 4599 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0001t0006 | 0/0 | 4599 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0001t0007 | 0/0 | 4599 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0003t0001 | 0/0 | 4599 | 6 | 6 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0005t0002 | 0/0 | 4599 | 3 | 0 | 0 | 0 | 0 | 3 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0008t0001 | 0/0 | 4599 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0010t0001 | 0/0 | 4599 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0001c0012t0002 | 0/0 | 4599 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002c0002t0001 | 0/0 | 4599 | 2 | 1 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002c0002t0003 | 0/0 | 4599 | 6 | 5 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0002c0006t0001 | 0/0 | 4599 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0003c0004t0001 | 0/0 | 4599 | 4 | 0 | 0 | 4 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0004c0011t0001 | 0/0 | 4599 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0005c0009t0002 | 0/0 | 4599 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0006c0007t0001 | 0/0 | 4599 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| a0007c0013t0001 | 0/0 | 4599 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | copy fasta | chr9 | 33285516 | 33376157 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0005t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0005t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0008t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0001c0012t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0006t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0002c0006t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0003c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0004c0011t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0005c0009t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0006c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| a0007c0013t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0179 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01109 | hp2 | a0001 | c0012 | t0002 | g0270 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0292 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01361 | hp2 | a0001 | c0008 | t0001 | g0123 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0174 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02132 | hp1 | a0006 | c0007 | t0001 | g0065 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02135 | hp1 | a0005 | c0009 | t0002 | g0284 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CDX | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02622 | hp2 | a0002 | c0006 | t0001 | g0177 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03130 | hp2 | a0002 | c0006 | t0001 | g0178 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03654 | hp1 | a0001 | c0005 | t0002 | g0223 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG04204 | hp1 | a0001 | c0005 | t0002 | g0221 | SAS | STU | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG04228 | hp2 | a0001 | c0005 | t0002 | g0248 | SAS | STU | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0171 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18950 | hp1 | a0003 | c0004 | t0001 | g0042 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18981 | hp2 | a0007 | c0013 | t0001 | g0126 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0040 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18995 | hp2 | a0004 | c0011 | t0001 | g0078 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19010 | hp2 | a0001 | c0010 | t0001 | g0077 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | LWK | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19060 | hp2 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19091 | hp1 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0180 | AFR | USA | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | USA | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0173 | AFR | LWK | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0090 | REF | REF | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0277 | REF | REF | NFX1_chr9_33285516_33376157 | NFX1 | chr9 | 33285516 | 33376157 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33294735
|
A | G | 1 | a0007 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.341A>G | p.His114Arg | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/24 | 398/4599 | 341/3363 | 114/1120 | chr9 | 33294735 | ||
| chr9:33328625
|
G | C | 1 | a0006 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1951G>C | p.Gly651Arg | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/24 | 2008/4599 | 1951/3363 | 651/1120 | chr9 | 33328625 | ||
| chr9:33342824
|
C | T | 1 | a0004 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.2194C>T | p.Arg732Cys | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/24 | 2251/4599 | 2194/3363 | 732/1120 | chr9 | 33342824 | ||
| chr9:33351711
|
C | T | 1 | a0002 | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
missense_variant | MODERATE | c.2576C>T | p.Pro859Leu | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 16/24 | 2633/4599 | 2576/3363 | 859/1120 | chr9 | 33351711 | ||
| chr9:33364766
|
G | T | 1 | a0005 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.3031G>T | p.Val1011Leu | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/24 | 3088/4599 | 3031/3363 | 1011/1120 | chr9 | 33364766 | ||
| chr9:33367586
|
C | A | 1 | a0003 | 4 | NA18950.hp1 NA18984.hp1 NA19060.hp2 others(1): Show |
missense_variant | MODERATE | c.3257C>A | p.Pro1086Gln | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/24 | 3314/4599 | 3257/3363 | 1086/1120 | chr9 | 33367586 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33318780
|
A | G | 1 | a0001c0012 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1638A>G | p.Val546Val | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 8/24 | 1695/4599 | 1638/3363 | 546/1120 | chr9 | 33318780 | ||
| chr9:33319060
|
A | G | 1 | a0001c0005 | 3 | HG03654.hp1 HG04204.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1839A>G | p.Lys613Lys | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/24 | 1896/4599 | 1839/3363 | 613/1120 | chr9 | 33319060 | ||
| chr9:33344160
|
C | T | 1 | a0001c0010 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.2316C>T | p.Cys772Cys | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/24 | 2373/4599 | 2316/3363 | 772/1120 | chr9 | 33344160 | ||
| chr9:33366646
|
A | G | 1 | a0001c0003 | 6 | HG02109.hp2 HG02896.hp1 HG03130.hp1 others(3): Show |
synonymous_variant | LOW | c.3057A>G | p.Lys1019Lys | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/24 | 3114/4599 | 3057/3363 | 1019/1120 | chr9 | 33366646 | ||
| chr9:33367551
|
T | C | 1 | a0002c0006 | 2 | HG02622.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.3222T>C | p.Gly1074Gly | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/24 | 3279/4599 | 3222/3363 | 1074/1120 | chr9 | 33367551 | ||
| chr9:33369945
|
G | A | 1 | a0001c0008 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.3330G>A | p.Glu1110Glu | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 3387/4599 | 3330/3363 | 1110/1120 | chr9 | 33369945 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33290534
|
A | G | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(11): Show | 224 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(221): Show |
5_prime_UTR_variant | MODIFIER | c.-39A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/24 | 39 | chr9 | 33290534 | |||||
| chr9:33370201
|
G | A | 1 | a0001c0001t0005 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 223 | chr9 | 33370201 | |||||
| chr9:33370239
|
C | T | 1 | a0001c0001t0007 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 261 | chr9 | 33370239 | |||||
| chr9:33370361
|
C | A | 1 | a0002c0002t0003 | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*383C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 383 | chr9 | 33370361 | |||||
| chr9:33370513
|
A | G | 1 | a0001c0001t0004 | 2 | HG02258.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 535 | chr9 | 33370513 | |||||
| chr9:33370710
|
A | G | 1 | a0001c0001t0006 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 24/24 | 732 | chr9 | 33370710 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:33290613
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02717.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.25+16G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33290613 | ||||||
| chr9:33290659
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.25+62G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33290659 | ||||||
| chr9:33290690
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.25+93G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33290690 | ||||||
| chr9:33290731
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.25+134G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33290731 | ||||||
| chr9:33291154
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.25+557C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291154 | ||||||
| chr9:33291522
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.25+925T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291522 | ||||||
| chr9:33291562
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25+965T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291562 | ||||||
| chr9:33291622
|
G | A | 1 | a0001c0005t0002g0221 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25+1025G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291622 | ||||||
| chr9:33291635
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.25+1038G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291635 | ||||||
| chr9:33291639
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.25+1042C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291639 | ||||||
| chr9:33291644
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.25+1047C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291644 | ||||||
| chr9:33291679
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.25+1082G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291679 | ||||||
| chr9:33291933
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25+1336G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33291933 | ||||||
| chr9:33292096
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.25+1499C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292096 | ||||||
| chr9:33292347
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.25+1750T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292347 | ||||||
| chr9:33292545
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-1875C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292545 | ||||||
| chr9:33292707
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.26-1713G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292707 | ||||||
| chr9:33292804
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.26-1616T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292804 | ||||||
| chr9:33292829
|
T | A | 1 | a0001c0001t0002g0222 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.26-1591T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292829 | ||||||
| chr9:33292932
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-1488C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33292932 | ||||||
| chr9:33293059
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0142a0001c0001t0001g0143others(15): Show | 20 | HG00280.hp2 HG00544.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-1361C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293059 | ||||||
| chr9:33293098
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0220others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-1322G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293098 | ||||||
| chr9:33293269
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-1151A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293269 | ||||||
| chr9:33293479
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.26-941A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293479 | ||||||
| chr9:33293482
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.26-938G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293482 | ||||||
| chr9:33293505
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-915A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293505 | ||||||
| chr9:33293885
|
G | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.26-535G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33293885 | ||||||
| chr9:33294039
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.26-381A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33294039 | ||||||
| chr9:33294093
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 213 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.26-327C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33294093 | ||||||
| chr9:33294182
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.26-238C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33294182 | ||||||
| chr9:33294370
|
A | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.26-50A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33294370 | ||||||
| chr9:33294400
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.26-20G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 1/23 | chr9 | 33294400 | ||||||
| chr9:33295502
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1033+75A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33295502 | ||||||
| chr9:33295581
|
C | T | 2 | a0002c0002t0003g0179a0002c0002t0003g0180 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1033+154C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33295581 | ||||||
| chr9:33295950
|
T | G | 1 | a0001c0001t0001g0034 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1033+523T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33295950 | ||||||
| chr9:33296114
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1033+687A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296114 | ||||||
| chr9:33296154
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1033+727T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296154 | ||||||
| chr9:33296725
|
C | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 217 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1033+1298C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296725 | ||||||
| chr9:33296732
|
A | G | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1033+1305A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296732 | ||||||
| chr9:33296786
|
G | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033+1359G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296786 | ||||||
| chr9:33296787
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1033+1360C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33296787 | ||||||
| chr9:33297430
|
G | A | 12 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1033+2003G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33297430 | ||||||
| chr9:33297637
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01433.hp2 HG01515.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1033+2210A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33297637 | ||||||
| chr9:33297714
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1033+2287A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33297714 | ||||||
| chr9:33297939
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG01496.hp1 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1033+2512C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33297939 | ||||||
| chr9:33298022
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1033+2595T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33298022 | ||||||
| chr9:33298111
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1033+2684G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33298111 | ||||||
| chr9:33298138
|
G | C | 12 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1033+2711G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33298138 | ||||||
| chr9:33298371
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02083.hp1 NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1034-2892C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33298371 | ||||||
| chr9:33298610
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0032 | 2 | HG02738.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1034-2653T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33298610 | ||||||
| chr9:33298783
|
CA | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-2469delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr9 | 33298783 | |||||
| chr9:33299080
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1034-2183G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33299080 | ||||||
| chr9:33299450
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01099.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1034-1813C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33299450 | ||||||
| chr9:33299757
|
T | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034-1506T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33299757 | ||||||
| chr9:33299997
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1034-1266C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33299997 | ||||||
| chr9:33300065
|
A | AT | 39 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1034-1172dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr9 | 33300065 | |||||
| chr9:33300065
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1034-1198A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33300065 | ||||||
| chr9:33300065
|
AT | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(38): Show | 41 | HG01074.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1034-1172delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr9 | 33300065 | |||||
| chr9:33300065
|
ATT | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(17): Show | 20 | HG02109.hp1 HG02129.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1034-1173_1034-117 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr9 | 33300065 | |||||
| chr9:33300413
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1034-850A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33300413 | ||||||
| chr9:33300464
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1034-799C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33300464 | ||||||
| chr9:33300664
|
C | T | 2 | a0002c0002t0001g0175a0002c0002t0001g0176 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1034-599C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33300664 | ||||||
| chr9:33300747
|
A | C | 1 | a0001c0001t0002g0279 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1034-516A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33300747 | ||||||
| chr9:33301087
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1034-176G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33301087 | ||||||
| chr9:33301100
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1034-163C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33301100 | ||||||
| chr9:33301244
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1034-19T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 2/23 | chr9 | 33301244 | ||||||
| chr9:33301553
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1192+132A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301553 | ||||||
| chr9:33301743
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0111a0001c0001t0001g0128 | 3 | HG00597.hp1 HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1192+322A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301743 | ||||||
| chr9:33301773
|
ATCT | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 164 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1192+359_1192+361d others(5): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr9 | 33301773 | |||||
| chr9:33301825
|
G | A | 4 | a0003c0004t0001g0040a0003c0004t0001g0041a0003c0004t0001g0042others(1): Show | 4 | NA18950.hp1 NA18984.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192+404G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301825 | ||||||
| chr9:33301851
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1192+430C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301851 | ||||||
| chr9:33301853
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1192+432T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301853 | ||||||
| chr9:33301870
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1192+449A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301870 | ||||||
| chr9:33301917
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1192+496T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33301917 | ||||||
| chr9:33302053
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1192+632C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302053 | ||||||
| chr9:33302357
|
A | AT | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1193-812dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr9 | 33302357 | |||||
| chr9:33302357
|
AT | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 241 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1193-812delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr9 | 33302357 | |||||
| chr9:33302357
|
ATT | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(30): Show | 33 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.1193-813_1193-812d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr9 | 33302357 | |||||
| chr9:33302441
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1193-750A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302441 | ||||||
| chr9:33302547
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1193-644C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302547 | ||||||
| chr9:33302587
|
C | T | 1 | a0001c0001t0007g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1193-604C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302587 | ||||||
| chr9:33302733
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1193-458G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302733 | ||||||
| chr9:33302882
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1193-309G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | chr9 | 33302882 | ||||||
| chr9:33302967
|
CT | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | HG01255.hp2 HG01256.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1193-205delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr9 | 33302967 | |||||
| chr9:33303328
|
G | A | 9 | a0001c0001t0002g0225a0001c0001t0002g0228a0001c0001t0002g0229others(6): Show | 9 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270+60G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303328 | ||||||
| chr9:33303351
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1270+83T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303351 | ||||||
| chr9:33303445
|
CCTGGCAA others(4): Show |
C | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1270+178_1270+188d others(13): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303445 | ||||||
| chr9:33303491
|
T | C | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1270+223T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303491 | ||||||
| chr9:33303902
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1270+634A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303902 | ||||||
| chr9:33303965
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1270+697G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303965 | ||||||
| chr9:33303988
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1270+720C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33303988 | ||||||
| chr9:33304130
|
T | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+862T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304130 | ||||||
| chr9:33304176
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1270+908C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304176 | ||||||
| chr9:33304240
|
C | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(7): Show | 10 | HG02071.hp2 HG02129.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1270+972C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304240 | ||||||
| chr9:33304240
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1270+972C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304240 | ||||||
| chr9:33304251
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1270+983G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304251 | ||||||
| chr9:33304253
|
C | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+985C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304253 | ||||||
| chr9:33304646
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1270+1378T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304646 | ||||||
| chr9:33304791
|
A | C | 1 | a0001c0012t0002g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270+1523A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304791 | ||||||
| chr9:33304796
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1270+1528A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304796 | ||||||
| chr9:33304803
|
A | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1270+1535A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304803 | ||||||
| chr9:33304951
|
G | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1270+1683G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33304951 | ||||||
| chr9:33305054
|
G | C | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1270+1786G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305054 | ||||||
| chr9:33305184
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270+1916A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305184 | ||||||
| chr9:33305459
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1271-1735G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305459 | ||||||
| chr9:33305575
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1271-1619G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305575 | ||||||
| chr9:33305601
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1271-1593T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305601 | ||||||
| chr9:33305655
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271-1539A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305655 | ||||||
| chr9:33305736
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1271-1458G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305736 | ||||||
| chr9:33305852
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1271-1342C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305852 | ||||||
| chr9:33305912
|
T | C | 6 | a0001c0001t0001g0186a0001c0003t0001g0183a0001c0003t0001g0184others(3): Show | 6 | HG02109.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1271-1282T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305912 | ||||||
| chr9:33305938
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1271-1256G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33305938 | ||||||
| chr9:33306011
|
T | G | 1 | a0001c0001t0002g0238 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1271-1183T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306011 | ||||||
| chr9:33306127
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1271-1067G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306127 | ||||||
| chr9:33306213
|
G | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(2): Show | 5 | HG01496.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-981G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306213 | ||||||
| chr9:33306251
|
G | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271-943G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306251 | ||||||
| chr9:33306338
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1271-856A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306338 | ||||||
| chr9:33306348
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1271-846A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306348 | ||||||
| chr9:33306352
|
C | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271-842C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306352 | ||||||
| chr9:33306374
|
C | T | 2 | a0001c0001t0002g0232a0001c0001t0002g0233 | 2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1271-820C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306374 | ||||||
| chr9:33306541
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1271-653A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306541 | ||||||
| chr9:33306699
|
A | G | 1 | a0001c0001t0002g0269 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1271-495A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306699 | ||||||
| chr9:33306974
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1271-220C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33306974 | ||||||
| chr9:33307024
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1271-170G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33307024 | ||||||
| chr9:33307046
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1271-148T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 4/23 | chr9 | 33307046 | ||||||
| chr9:33307440
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18974.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1376+141G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307440 | ||||||
| chr9:33307562
|
T | G | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1376+263T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307562 | ||||||
| chr9:33307571
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1376+272G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307571 | ||||||
| chr9:33307722
|
A | C | 1 | a0007c0013t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1376+423A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307722 | ||||||
| chr9:33307790
|
CTTTCT | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1376+495_1376+499d others(7): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr9 | 33307790 | |||||
| chr9:33307790
|
CTTTCTT | C | 8 | a0001c0001t0001g0163a0001c0001t0001g0186a0001c0001t0001g0189others(5): Show | 8 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376+495_1376+500d others(8): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr9 | 33307790 | |||||
| chr9:33307794
|
CT | C | 118 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 119 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.1376+516delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr9 | 33307794 | |||||
| chr9:33307794
|
CTT | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 151 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1376+515_1376+516d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr9 | 33307794 | |||||
| chr9:33307800
|
T | C | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+501T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307800 | ||||||
| chr9:33307890
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1376+591G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307890 | ||||||
| chr9:33307989
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1376+690G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33307989 | ||||||
| chr9:33308051
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1376+752C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308051 | ||||||
| chr9:33308072
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+773C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308072 | ||||||
| chr9:33308170
|
G | A | 5 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01255.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376+871G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308170 | ||||||
| chr9:33308269
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1376+970C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308269 | ||||||
| chr9:33308315
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1376+1016A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308315 | ||||||
| chr9:33308343
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1376+1044G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308343 | ||||||
| chr9:33308418
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1376+1119G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308418 | ||||||
| chr9:33308492
|
A | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | HG02083.hp1 HG03492.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376+1193A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308492 | ||||||
| chr9:33308648
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0031 | 2 | NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1376+1349G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308648 | ||||||
| chr9:33308720
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1376+1421C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308720 | ||||||
| chr9:33308859
|
G | A | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376+1560G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33308859 | ||||||
| chr9:33309041
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1376+1742A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309041 | ||||||
| chr9:33309126
|
G | A | 1 | a0001c0001t0002g0243 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1376+1827G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309126 | ||||||
| chr9:33309351
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1377-1755C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309351 | ||||||
| chr9:33309360
|
GA | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1377-1732delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr9 | 33309360 | |||||
| chr9:33309370
|
A | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1377-1736A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309370 | ||||||
| chr9:33309695
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377-1411G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309695 | ||||||
| chr9:33309915
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1377-1191T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33309915 | ||||||
| chr9:33310217
|
C | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377-889C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310217 | ||||||
| chr9:33310254
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1377-852G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310254 | ||||||
| chr9:33310597
|
T | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1377-509T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310597 | ||||||
| chr9:33310684
|
G | A | 6 | a0001c0001t0001g0186a0001c0003t0001g0183a0001c0003t0001g0184others(3): Show | 6 | HG02109.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377-422G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310684 | ||||||
| chr9:33310746
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1377-360A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310746 | ||||||
| chr9:33310995
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1377-111G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33310995 | ||||||
| chr9:33311102
|
T | C | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1377-4T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 5/23 | chr9 | 33311102 | ||||||
| chr9:33311299
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1448+122T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311299 | ||||||
| chr9:33311557
|
A | AT | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 43 | HG00408.hp1 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1448+393dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr9 | 33311557 | |||||
| chr9:33311621
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1448+444C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311621 | ||||||
| chr9:33311626
|
C | A | 2 | a0001c0001t0002g0282a0001c0001t0002g0291 | 2 | NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1448+449C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311626 | ||||||
| chr9:33311697
|
C | T | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1448+520C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311697 | ||||||
| chr9:33311706
|
C | T | 5 | a0001c0001t0002g0242a0001c0001t0002g0266a0001c0001t0002g0267others(2): Show | 5 | HG00408.hp1 HG02155.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1448+529C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311706 | ||||||
| chr9:33311836
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1448+659C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311836 | ||||||
| chr9:33311840
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1448+663C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311840 | ||||||
| chr9:33311966
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448+789G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33311966 | ||||||
| chr9:33312116
|
T | C | 2 | a0002c0006t0001g0177a0002c0006t0001g0178 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1448+939T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312116 | ||||||
| chr9:33312216
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1448+1039A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312216 | ||||||
| chr9:33312363
|
A | G | 1 | a0001c0005t0002g0221 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1448+1186A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312363 | ||||||
| chr9:33312442
|
A | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0162a0001c0001t0001g0165others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449-1212A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312442 | ||||||
| chr9:33312636
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1449-1018C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312636 | ||||||
| chr9:33312646
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1449-1008G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312646 | ||||||
| chr9:33312668
|
C | T | 12 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1449-986C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312668 | ||||||
| chr9:33312688
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0045others(38): Show | 43 | HG00280.hp2 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1449-966T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33312688 | ||||||
| chr9:33313327
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(6): Show | 9 | HG01123.hp1 HG04204.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.1449-327G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33313327 | ||||||
| chr9:33313368
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1449-286C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33313368 | ||||||
| chr9:33313427
|
T | TA | 10 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1449-216dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr9 | 33313427 | |||||
| chr9:33313542
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1449-112T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33313542 | ||||||
| chr9:33313567
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1449-87G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 6/23 | chr9 | 33313567 | ||||||
| chr9:33314157
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1588+364T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33314157 | ||||||
| chr9:33314448
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1588+655C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33314448 | ||||||
| chr9:33314667
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588+874G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33314667 | ||||||
| chr9:33314975
|
A | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1588+1182A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33314975 | ||||||
| chr9:33315225
|
C | CAA | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1588+1447_1588+144 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315225 | |||||
| chr9:33315225
|
CA | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(9): Show | 12 | HG00639.hp1 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1588+1448delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315225 | |||||
| chr9:33315449
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1588+1656C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315449 | ||||||
| chr9:33315453
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1588+1660G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315453 | ||||||
| chr9:33315628
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1588+1835G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315628 | ||||||
| chr9:33315667
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+1874A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315667 | ||||||
| chr9:33315724
|
C | CA | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(82): Show | 87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1588+1933dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315724 | |||||
| chr9:33315724
|
C | CAA | 3 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0044 | 3 | HG02080.hp2 HG06807.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1588+1932_1588+193 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315724 | |||||
| chr9:33315727
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 220 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1588+1934C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315727 | ||||||
| chr9:33315730
|
C | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 221 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1588+1937C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315730 | ||||||
| chr9:33315733
|
A | C | 6 | a0001c0001t0002g0224a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG02683.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+1940A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315733 | ||||||
| chr9:33315891
|
C | CA | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 160 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.1588+2110dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315891 | |||||
| chr9:33315891
|
C | CAA | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 135 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1588+2109_1588+211 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33315891 | |||||
| chr9:33315924
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1588+2131A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315924 | ||||||
| chr9:33315974
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(7): Show | 10 | HG02071.hp2 HG02129.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588+2181G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315974 | ||||||
| chr9:33315977
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1588+2184G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33315977 | ||||||
| chr9:33316057
|
T | C | 1 | a0001c0003t0001g0183 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1588+2264T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316057 | ||||||
| chr9:33316108
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1588+2315G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316108 | ||||||
| chr9:33316311
|
C | CT | 6 | a0001c0001t0001g0026a0001c0001t0001g0133a0001c0001t0001g0189others(3): Show | 6 | HG02258.hp1 HG03453.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-2406dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33316311 | |||||
| chr9:33316497
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1589-2234G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316497 | ||||||
| chr9:33316517
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-2214C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316517 | ||||||
| chr9:33316622
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1589-2109C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316622 | ||||||
| chr9:33316667
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1589-2064T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316667 | ||||||
| chr9:33316905
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1589-1826C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316905 | ||||||
| chr9:33316996
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1589-1735G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33316996 | ||||||
| chr9:33317116
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1589-1615C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317116 | ||||||
| chr9:33317177
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 217 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1589-1554A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317177 | ||||||
| chr9:33317343
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1589-1388C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317343 | ||||||
| chr9:33317419
|
C | CA | 9 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.1589-1296dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317419 | |||||
| chr9:33317419
|
C | CAAAAA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.1589-1300_1589-129 others(9): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317419 | |||||
| chr9:33317432
|
A | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1589-1299A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317432 | ||||||
| chr9:33317435
|
AG | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG00642.hp1 HG01123.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1589-1295delG | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317435 | ||||||
| chr9:33317436
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 208 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1589-1295G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317436 | ||||||
| chr9:33317460
|
G | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1589-1271G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317460 | ||||||
| chr9:33317473
|
C | G | 1 | a0002c0002t0003g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1589-1258C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317473 | ||||||
| chr9:33317533
|
T | TA | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-1186dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317533 | |||||
| chr9:33317630
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1589-1101C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317630 | ||||||
| chr9:33317663
|
T | TA | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1589-1055dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317663 | |||||
| chr9:33317688
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1589-1043A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317688 | ||||||
| chr9:33317705
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1589-1026G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317705 | ||||||
| chr9:33317792
|
G | A | 1 | a0001c0012t0002g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1589-939G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317792 | ||||||
| chr9:33317831
|
C | G | 1 | a0001c0001t0002g0255 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1589-900C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317831 | ||||||
| chr9:33317845
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | NA18961.hp2 NA18978.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1589-886G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33317845 | ||||||
| chr9:33317973
|
C | CA | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 131 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1589-730dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317973 | |||||
| chr9:33317973
|
C | CAA | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1589-731_1589-730d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317973 | |||||
| chr9:33317973
|
C | CAAA | 15 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(12): Show | 15 | HG02055.hp2 HG02622.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1589-732_1589-730d others(5): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317973 | |||||
| chr9:33317973
|
C | CAAAA | 9 | a0001c0001t0001g0008a0001c0001t0001g0148a0001c0001t0001g0181others(6): Show | 9 | HG02071.hp2 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1589-733_1589-730d others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317973 | |||||
| chr9:33317973
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1589-740_1589-730d others(13): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr9 | 33317973 | |||||
| chr9:33318104
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.1589-627G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318104 | ||||||
| chr9:33318169
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1589-562T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318169 | ||||||
| chr9:33318206
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1589-525G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318206 | ||||||
| chr9:33318390
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1589-341G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318390 | ||||||
| chr9:33318538
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01433.hp2 HG01515.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1589-193C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318538 | ||||||
| chr9:33318590
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1589-141A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 7/23 | chr9 | 33318590 | ||||||
| chr9:33318877
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02717.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1689-33C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 8/23 | chr9 | 33318877 | ||||||
| chr9:33319258
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1906+131T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319258 | ||||||
| chr9:33319335
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1906+208G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319335 | ||||||
| chr9:33319351
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1906+224C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319351 | ||||||
| chr9:33319415
|
G | A | 4 | a0001c0001t0002g0247a0001c0005t0002g0221a0001c0005t0002g0223others(1): Show | 4 | HG02132.hp2 HG03654.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+288G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319415 | ||||||
| chr9:33319540
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1906+413C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319540 | ||||||
| chr9:33319549
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1906+422G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319549 | ||||||
| chr9:33319650
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1906+523C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319650 | ||||||
| chr9:33319666
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1906+539C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319666 | ||||||
| chr9:33319670
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1906+543C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319670 | ||||||
| chr9:33319907
|
C | T | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+780C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319907 | ||||||
| chr9:33319965
|
C | CT | 6 | a0001c0001t0001g0088a0001c0001t0001g0124a0001c0001t0001g0148others(3): Show | 6 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+852dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33319965 | |||||
| chr9:33319965
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1906+838C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319965 | ||||||
| chr9:33319992
|
C | T | 2 | a0001c0001t0002g0269a0001c0001t0002g0290 | 2 | NA18947.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1906+865C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33319992 | ||||||
| chr9:33320117
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1906+990A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320117 | ||||||
| chr9:33320154
|
G | A | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+1027G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320154 | ||||||
| chr9:33320361
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(6): Show | 9 | HG01123.hp1 HG04204.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.1906+1234A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320361 | ||||||
| chr9:33320389
|
A | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02717.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1906+1262A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320389 | ||||||
| chr9:33320461
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1906+1334G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320461 | ||||||
| chr9:33320747
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1906+1620G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320747 | ||||||
| chr9:33320769
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1906+1642A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33320769 | ||||||
| chr9:33321013
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1906+1886C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321013 | ||||||
| chr9:33321052
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1906+1925A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321052 | ||||||
| chr9:33321078
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1906+1951G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321078 | ||||||
| chr9:33321110
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1906+1983C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321110 | ||||||
| chr9:33321484
|
GAGACTGG others(9): Show |
G | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+2358_1906+237 others(20): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321484 | ||||||
| chr9:33321502
|
ACT | A | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+2376_1906+237 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33321502 | ||||||
| chr9:33321878
|
C | CA | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1906+2768dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33321878 | |||||
| chr9:33322046
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1906+2919C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33322046 | ||||||
| chr9:33322201
|
GA | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1906+3090delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33322201 | |||||
| chr9:33322542
|
T | C | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+3415T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33322542 | ||||||
| chr9:33322730
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02717.hp2 HG02723.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+3603C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33322730 | ||||||
| chr9:33322925
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1906+3798T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33322925 | ||||||
| chr9:33323167
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1906+4040A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323167 | ||||||
| chr9:33323344
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1906+4217A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323344 | ||||||
| chr9:33323668
|
C | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 291 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1906+4541C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323668 | ||||||
| chr9:33323702
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+4575G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323702 | ||||||
| chr9:33323703
|
C | T | 1 | a0001c0001t0007g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1906+4576C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323703 | ||||||
| chr9:33323760
|
A | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 30 | HG00408.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1906+4633A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323760 | ||||||
| chr9:33323763
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1906+4636A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323763 | ||||||
| chr9:33323778
|
CAAAT | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0119a0001c0001t0001g0127others(1): Show | 4 | HG01106.hp1 HG02738.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+4661_1906+466 others(8): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33323778 | |||||
| chr9:33323818
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1906+4691A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323818 | ||||||
| chr9:33323942
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1907-4639C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323942 | ||||||
| chr9:33323943
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1907-4638G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33323943 | ||||||
| chr9:33324244
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1907-4337C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324244 | ||||||
| chr9:33324244
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 167 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.1907-4337C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324244 | ||||||
| chr9:33324544
|
T | G | 35 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1907-4037T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324544 | ||||||
| chr9:33324581
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1907-4000C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324581 | ||||||
| chr9:33324581
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0071 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1907-4000C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324581 | ||||||
| chr9:33324703
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907-3878G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33324703 | ||||||
| chr9:33324928
|
C | CA | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG01109.hp1 HG02258.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1907-3638dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33324928 | |||||
| chr9:33325029
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1907-3552C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33325029 | ||||||
| chr9:33325112
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1907-3469C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33325112 | ||||||
| chr9:33325418
|
CTT | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 127 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1907-3161_1907-316 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33325418 | |||||
| chr9:33325586
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1907-2995C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33325586 | ||||||
| chr9:33325654
|
ACT | A | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907-2924_1907-292 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33325654 | |||||
| chr9:33325789
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1907-2792C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33325789 | ||||||
| chr9:33325829
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1907-2752T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33325829 | ||||||
| chr9:33326286
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1907-2295G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326286 | ||||||
| chr9:33326413
|
T | TA | 36 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 36 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1907-2144dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33326413 | |||||
| chr9:33326413
|
TA | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0097others(5): Show | 8 | HG01069.hp1 HG01074.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1907-2144delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr9 | 33326413 | |||||
| chr9:33326451
|
G | T | 1 | a0001c0010t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1907-2130G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326451 | ||||||
| chr9:33326481
|
G | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1907-2100G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326481 | ||||||
| chr9:33326565
|
G | C | 49 | a0001c0001t0002g0004a0001c0001t0002g0222a0001c0001t0002g0224others(46): Show | 50 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1907-2016G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326565 | ||||||
| chr9:33326583
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1907-1998G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326583 | ||||||
| chr9:33326687
|
C | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1907-1894C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326687 | ||||||
| chr9:33326887
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1907-1694G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326887 | ||||||
| chr9:33326934
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1907-1647A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33326934 | ||||||
| chr9:33327244
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-1337C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33327244 | ||||||
| chr9:33327430
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1907-1151T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33327430 | ||||||
| chr9:33327446
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1907-1135C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33327446 | ||||||
| chr9:33327509
|
T | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1907-1072T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33327509 | ||||||
| chr9:33327640
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1907-941C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33327640 | ||||||
| chr9:33328060
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1907-521G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33328060 | ||||||
| chr9:33328217
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1907-364G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 9/23 | chr9 | 33328217 | ||||||
| chr9:33328788
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2004+110T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33328788 | ||||||
| chr9:33328814
|
A | G | 35 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2004+136A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33328814 | ||||||
| chr9:33328930
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2004+252C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33328930 | ||||||
| chr9:33329007
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004+329G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329007 | ||||||
| chr9:33329084
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2004+406G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329084 | ||||||
| chr9:33329163
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004+485A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329163 | ||||||
| chr9:33329247
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004+569A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329247 | ||||||
| chr9:33329300
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2004+622T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329300 | ||||||
| chr9:33329312
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2004+634T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329312 | ||||||
| chr9:33329371
|
G | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG02258.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2004+693G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329371 | ||||||
| chr9:33329644
|
CT | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 221 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.2004+979delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr9 | 33329644 | |||||
| chr9:33329667
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2004+989T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329667 | ||||||
| chr9:33329881
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004+1203A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329881 | ||||||
| chr9:33329975
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2004+1297G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33329975 | ||||||
| chr9:33330041
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2004+1363G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330041 | ||||||
| chr9:33330114
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004+1436A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330114 | ||||||
| chr9:33330313
|
G | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004+1635G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330313 | ||||||
| chr9:33330399
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 127 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.2004+1721C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330399 | ||||||
| chr9:33330419
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2004+1741A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330419 | ||||||
| chr9:33330430
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 126 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2004+1752G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330430 | ||||||
| chr9:33330455
|
A | G | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+1777A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330455 | ||||||
| chr9:33330569
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0108 | 2 | HG03239.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2004+1891T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330569 | ||||||
| chr9:33330783
|
T | C | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2005-1689T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330783 | ||||||
| chr9:33330876
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2005-1596C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330876 | ||||||
| chr9:33330894
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2005-1578A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33330894 | ||||||
| chr9:33331046
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2005-1426G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33331046 | ||||||
| chr9:33331694
|
C | CT | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(32): Show | 35 | HG01255.hp2 HG01361.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.2005-763dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr9 | 33331694 | |||||
| chr9:33331694
|
C | CTT | 22 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG01123.hp1 HG02071.hp2 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.2005-764_2005-763d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr9 | 33331694 | |||||
| chr9:33331948
|
G | A | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2005-524G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33331948 | ||||||
| chr9:33332045
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01081.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2005-427G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332045 | ||||||
| chr9:33332076
|
C | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(2): Show | 5 | HG01496.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2005-396C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332076 | ||||||
| chr9:33332129
|
T | G | 1 | a0001c0001t0002g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2005-343T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332129 | ||||||
| chr9:33332143
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2005-329C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332143 | ||||||
| chr9:33332163
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2005-309C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332163 | ||||||
| chr9:33332268
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2005-204T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 10/23 | chr9 | 33332268 | ||||||
| chr9:33332556
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2035+54T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332556 | ||||||
| chr9:33332852
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2035+350C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332852 | ||||||
| chr9:33332876
|
C | G | 1 | a0001c0001t0002g0241 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2035+374C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332876 | ||||||
| chr9:33332887
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG01071.hp1 HG02615.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.2035+385G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332887 | ||||||
| chr9:33332974
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2035+472T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332974 | ||||||
| chr9:33332987
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0001g0102 | 4 | HG01081.hp2 HG01257.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2035+485A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332987 | ||||||
| chr9:33332995
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2035+493A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33332995 | ||||||
| chr9:33333095
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2035+593C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333095 | ||||||
| chr9:33333098
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2035+596G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333098 | ||||||
| chr9:33333126
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2035+624A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333126 | ||||||
| chr9:33333134
|
CCA | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2035+636_2035+637d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33333134 | |||||
| chr9:33333347
|
C | T | 2 | a0002c0006t0001g0177a0002c0006t0001g0178 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2035+845C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333347 | ||||||
| chr9:33333604
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2035+1102T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333604 | ||||||
| chr9:33333650
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2035+1148G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333650 | ||||||
| chr9:33333789
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2035+1287C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333789 | ||||||
| chr9:33333831
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2035+1329A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333831 | ||||||
| chr9:33333883
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0122 | 2 | NA18990.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2035+1381G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333883 | ||||||
| chr9:33333920
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2035+1418G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333920 | ||||||
| chr9:33333944
|
A | T | 5 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01255.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2035+1442A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33333944 | ||||||
| chr9:33334008
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.2035+1506A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334008 | ||||||
| chr9:33334018
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 218 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.2035+1516C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334018 | ||||||
| chr9:33334087
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2035+1585G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334087 | ||||||
| chr9:33334103
|
C | T | 5 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0220others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2035+1601C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334103 | ||||||
| chr9:33334107
|
TGCTCTCC others(7): Show |
T | 1 | a0001c0001t0002g0227 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2035+1608_2035+162 others(18): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33334107 | |||||
| chr9:33334218
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.2035+1716G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334218 | ||||||
| chr9:33334427
|
T | G | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2035+1925T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334427 | ||||||
| chr9:33334469
|
A | C | 1 | a0001c0012t0002g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2035+1967A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334469 | ||||||
| chr9:33334516
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2035+2014T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334516 | ||||||
| chr9:33334713
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2035+2211G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334713 | ||||||
| chr9:33334835
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.2035+2333T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334835 | ||||||
| chr9:33334959
|
A | C | 33 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(30): Show | 33 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2035+2457A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334959 | ||||||
| chr9:33334980
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2035+2478C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33334980 | ||||||
| chr9:33335112
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 137 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2035+2610A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335112 | ||||||
| chr9:33335215
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2035+2713A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335215 | ||||||
| chr9:33335227
|
C | CT | 22 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0030others(19): Show | 22 | HG00639.hp1 HG02071.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2035+2745dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33335227 | |||||
| chr9:33335227
|
CTT | C | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2035+2744_2035+274 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33335227 | |||||
| chr9:33335232
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2035+2730T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335232 | ||||||
| chr9:33335254
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2035+2752G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335254 | ||||||
| chr9:33335332
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2035+2830G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335332 | ||||||
| chr9:33335412
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2035+2910T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335412 | ||||||
| chr9:33335636
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2036-2874C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335636 | ||||||
| chr9:33335935
|
G | A | 1 | a0001c0003t0001g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2036-2575G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33335935 | ||||||
| chr9:33336246
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2036-2264C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336246 | ||||||
| chr9:33336276
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2036-2234C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336276 | ||||||
| chr9:33336372
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2036-2138C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336372 | ||||||
| chr9:33336376
|
C | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0181others(4): Show | 7 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2036-2134C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336376 | ||||||
| chr9:33336480
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0069 | 3 | HG01081.hp2 HG01257.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2036-2030C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336480 | ||||||
| chr9:33336562
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2036-1948C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336562 | ||||||
| chr9:33336717
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 224 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.2036-1793A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336717 | ||||||
| chr9:33336725
|
CA | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2036-1782delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33336725 | |||||
| chr9:33336828
|
G | A | 5 | a0001c0001t0001g0165a0002c0002t0001g0175a0002c0002t0001g0176others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2036-1682G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336828 | ||||||
| chr9:33336856
|
C | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2036-1654C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336856 | ||||||
| chr9:33336876
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2036-1634C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336876 | ||||||
| chr9:33336959
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2036-1551C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33336959 | ||||||
| chr9:33337083
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2036-1427G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337083 | ||||||
| chr9:33337195
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2036-1315A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337195 | ||||||
| chr9:33337650
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2036-860G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337650 | ||||||
| chr9:33337651
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 217 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.2036-859T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337651 | ||||||
| chr9:33337655
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0220 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2036-855G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337655 | ||||||
| chr9:33337684
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2036-826A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337684 | ||||||
| chr9:33337731
|
TAAAACAA others(3): Show |
T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.2036-759_2036-750d others(12): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr9 | 33337731 | |||||
| chr9:33337778
|
G | T | 3 | a0001c0005t0002g0221a0001c0005t0002g0223a0001c0005t0002g0248 | 3 | HG03654.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2036-732G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337778 | ||||||
| chr9:33337916
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2036-594G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337916 | ||||||
| chr9:33337964
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2036-546G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33337964 | ||||||
| chr9:33338303
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2036-207C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33338303 | ||||||
| chr9:33338334
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2036-176G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 11/23 | chr9 | 33338334 | ||||||
| chr9:33338631
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2115+42G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33338631 | ||||||
| chr9:33338691
|
TG | T | 10 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0003g0171others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2115+105delG | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33338691 | |||||
| chr9:33338722
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2115+133C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33338722 | ||||||
| chr9:33339007
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2115+418T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33339007 | ||||||
| chr9:33339130
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2115+541C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33339130 | ||||||
| chr9:33339911
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2115+1322A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33339911 | ||||||
| chr9:33340042
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+1453C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340042 | ||||||
| chr9:33340166
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2115+1577G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340166 | ||||||
| chr9:33340276
|
G | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+1687G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340276 | ||||||
| chr9:33340400
|
C | T | 1 | a0001c0003t0001g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2115+1811C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340400 | ||||||
| chr9:33340602
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2115+2013A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340602 | ||||||
| chr9:33340824
|
A | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0286 | 3 | HG02809.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2116-1922A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33340824 | ||||||
| chr9:33341428
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2116-1318G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341428 | ||||||
| chr9:33341664
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2116-1082C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341664 | ||||||
| chr9:33341693
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2116-1053C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341693 | ||||||
| chr9:33341727
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2116-1019C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341727 | ||||||
| chr9:33341793
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2116-953A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341793 | ||||||
| chr9:33341805
|
C | CTAAA | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2116-934_2116-931d others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33341805 | |||||
| chr9:33341844
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(6): Show | 9 | HG01123.hp1 HG04204.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.2116-902C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33341844 | ||||||
| chr9:33341871
|
CT | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02717.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2116-872delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33341871 | |||||
| chr9:33342080
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2116-666C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33342080 | ||||||
| chr9:33342128
|
T | TCA | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0056others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2116-596_2116-595d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33342128 | |||||
| chr9:33342128
|
T | TCACACAC others(3): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2116-604_2116-595d others(12): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33342128 | |||||
| chr9:33342128
|
TCA | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2116-596_2116-595d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33342128 | |||||
| chr9:33342130
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2116-616A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33342130 | ||||||
| chr9:33342205
|
ACC | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2116-536_2116-535d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr9 | 33342205 | |||||
| chr9:33342277
|
C | T | 32 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0043others(29): Show | 32 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.2116-469C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33342277 | ||||||
| chr9:33342692
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2116-54G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 12/23 | chr9 | 33342692 | ||||||
| chr9:33343051
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2224+197A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343051 | ||||||
| chr9:33343103
|
A | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2224+249A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343103 | ||||||
| chr9:33343112
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2224+258A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343112 | ||||||
| chr9:33343129
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2224+275G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343129 | ||||||
| chr9:33343177
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2224+323C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343177 | ||||||
| chr9:33343179
|
A | G | 7 | a0001c0001t0002g0224a0001c0001t0002g0244a0001c0001t0002g0251others(4): Show | 7 | HG01358.hp1 HG01433.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2224+325A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343179 | ||||||
| chr9:33343362
|
T | A | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2224+508T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343362 | ||||||
| chr9:33343365
|
A | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2224+511A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343365 | ||||||
| chr9:33343399
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 102 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2224+545G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343399 | ||||||
| chr9:33343452
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2224+598G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343452 | ||||||
| chr9:33343812
|
T | A | 1 | a0001c0001t0002g0259 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2225-257T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33343812 | ||||||
| chr9:33344045
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2225-24T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 13/23 | chr9 | 33344045 | ||||||
| chr9:33344196
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.2344+8C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33344196 | ||||||
| chr9:33344254
|
T | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2344+66T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33344254 | ||||||
| chr9:33344366
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2344+178T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33344366 | ||||||
| chr9:33344739
|
G | A | 11 | a0001c0001t0002g0251a0002c0002t0001g0175a0002c0002t0001g0176others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344+551G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33344739 | ||||||
| chr9:33344857
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2344+669T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33344857 | ||||||
| chr9:33345012
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2344+824G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345012 | ||||||
| chr9:33345031
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2344+843G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345031 | ||||||
| chr9:33345152
|
A | T | 1 | a0001c0001t0002g0247 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2344+964A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345152 | ||||||
| chr9:33345169
|
GAAAAGA | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2344+998_2344+1003 others(9): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr9 | 33345169 | |||||
| chr9:33345212
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2344+1024C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345212 | ||||||
| chr9:33345345
|
T | C | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2344+1157T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345345 | ||||||
| chr9:33345425
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+1237C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345425 | ||||||
| chr9:33345459
|
A | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2344+1271A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345459 | ||||||
| chr9:33345618
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.2345-1420A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345618 | ||||||
| chr9:33345632
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2345-1406A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345632 | ||||||
| chr9:33345663
|
T | TC | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345-1372dupC | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr9 | 33345663 | |||||
| chr9:33345714
|
A | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(36): Show | 39 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2345-1324A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345714 | ||||||
| chr9:33345889
|
A | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(2): Show | 5 | HG01496.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2345-1149A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345889 | ||||||
| chr9:33345965
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0031 | 3 | NA18974.hp1 NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2345-1073A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33345965 | ||||||
| chr9:33346021
|
A | C | 18 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0201others(15): Show | 18 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2345-1017A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346021 | ||||||
| chr9:33346139
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2345-899G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346139 | ||||||
| chr9:33346199
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0134 | 3 | HG01099.hp1 HG01975.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2345-839C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346199 | ||||||
| chr9:33346206
|
G | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2345-832G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346206 | ||||||
| chr9:33346432
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2345-606C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346432 | ||||||
| chr9:33346560
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2345-478C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346560 | ||||||
| chr9:33346812
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2345-226G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346812 | ||||||
| chr9:33346860
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2345-178G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 14/23 | chr9 | 33346860 | ||||||
| chr9:33347476
|
A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2424+359A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33347476 | ||||||
| chr9:33347485
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0139 | 4 | HG02155.hp1 NA18939.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2424+368T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33347485 | ||||||
| chr9:33347499
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2424+382T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33347499 | ||||||
| chr9:33347808
|
G | C | 1 | a0001c0001t0002g0228 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2424+691G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33347808 | ||||||
| chr9:33348018
|
A | ACT | 5 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0220others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2424+904_2424+905d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr9 | 33348018 | |||||
| chr9:33348031
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2424+914G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33348031 | ||||||
| chr9:33348185
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2424+1068T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33348185 | ||||||
| chr9:33348383
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2424+1266T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33348383 | ||||||
| chr9:33348469
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2424+1352C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33348469 | ||||||
| chr9:33348505
|
G | GA | 9 | a0002c0002t0001g0175a0002c0002t0003g0171a0002c0002t0003g0172others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2424+1400dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr9 | 33348505 | |||||
| chr9:33348505
|
GA | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 126 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2424+1400delA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr9 | 33348505 | |||||
| chr9:33348665
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2424+1548A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33348665 | ||||||
| chr9:33348879
|
C | CA | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2424+1773dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr9 | 33348879 | |||||
| chr9:33349102
|
G | C | 1 | a0001c0001t0002g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2424+1985G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349102 | ||||||
| chr9:33349168
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2424+2051A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349168 | ||||||
| chr9:33349211
|
C | T | 2 | a0001c0001t0002g0262a0001c0001t0002g0271 | 2 | NA18956.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2424+2094C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349211 | ||||||
| chr9:33349611
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2425-1949C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349611 | ||||||
| chr9:33349653
|
G | A | 2 | a0002c0002t0001g0175a0002c0002t0001g0176 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2425-1907G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349653 | ||||||
| chr9:33349703
|
C | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2425-1857C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349703 | ||||||
| chr9:33349773
|
T | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(36): Show | 39 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2425-1787T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349773 | ||||||
| chr9:33349781
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2425-1779G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349781 | ||||||
| chr9:33349966
|
A | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG02258.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2425-1594A>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33349966 | ||||||
| chr9:33350028
|
G | A | 1 | a0001c0012t0002g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2425-1532G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350028 | ||||||
| chr9:33350217
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2425-1343T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350217 | ||||||
| chr9:33350220
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2425-1340C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350220 | ||||||
| chr9:33350303
|
C | CA | 12 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0066others(9): Show | 12 | HG00735.hp2 HG02145.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2425-1239dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr9 | 33350303 | |||||
| chr9:33350459
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2425-1101C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350459 | ||||||
| chr9:33350568
|
G | T | 3 | a0001c0001t0001g0165a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG02258.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2425-992G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350568 | ||||||
| chr9:33350577
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2425-983T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350577 | ||||||
| chr9:33350588
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2425-972A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350588 | ||||||
| chr9:33350709
|
A | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425-851A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350709 | ||||||
| chr9:33350755
|
C | G | 18 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0201others(15): Show | 18 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2425-805C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33350755 | ||||||
| chr9:33351011
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425-549G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33351011 | ||||||
| chr9:33351142
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2425-418G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33351142 | ||||||
| chr9:33351228
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2425-332C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33351228 | ||||||
| chr9:33351245
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2425-315C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33351245 | ||||||
| chr9:33351260
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0119others(2): Show | 5 | HG01106.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425-300C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 15/23 | chr9 | 33351260 | ||||||
| chr9:33352311
|
TGTGGAGT others(4): Show |
T | 1 | a0001c0001t0001g0051 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2656-334_2656-324d others(13): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 16/23 | chr9 | 33352311 | ||||||
| chr9:33352332
|
GCTAGGCC others(49): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2656-306_2656-251d others(58): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr9 | 33352332 | |||||
| chr9:33352452
|
C | T | 5 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG01255.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2656-194C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 16/23 | chr9 | 33352452 | ||||||
| chr9:33352462
|
C | A | 1 | a0001c0001t0002g0263 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2656-184C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 16/23 | chr9 | 33352462 | ||||||
| chr9:33352738
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2729+19T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33352738 | ||||||
| chr9:33352739
|
TAAC | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2729+24_2729+26del others(3): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr9 | 33352739 | |||||
| chr9:33352828
|
C | CAAA | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2729+109_2729+110i others(5): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33352828 | ||||||
| chr9:33352889
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2729+170T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33352889 | ||||||
| chr9:33352965
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2729+246G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33352965 | ||||||
| chr9:33352979
|
G | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2729+260G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33352979 | ||||||
| chr9:33353004
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2729+285A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353004 | ||||||
| chr9:33353023
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2729+304G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353023 | ||||||
| chr9:33353179
|
CTTTT | C | 5 | a0001c0003t0001g0183a0001c0003t0001g0184a0001c0003t0001g0185others(2): Show | 5 | HG02896.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2729+464_2729+467d others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr9 | 33353179 | |||||
| chr9:33353214
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.2729+495G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353214 | ||||||
| chr9:33353304
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2729+585C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353304 | ||||||
| chr9:33353347
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2729+628A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353347 | ||||||
| chr9:33353362
|
T | C | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2729+643T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353362 | ||||||
| chr9:33353377
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2729+658C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353377 | ||||||
| chr9:33353561
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2730-525G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353561 | ||||||
| chr9:33353683
|
C | CT | 43 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2730-381dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr9 | 33353683 | |||||
| chr9:33353683
|
CT | C | 11 | a0001c0001t0001g0100a0001c0001t0001g0135a0001c0001t0001g0144others(8): Show | 11 | HG01515.hp2 HG01517.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.2730-381delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr9 | 33353683 | |||||
| chr9:33353719
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2730-367G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353719 | ||||||
| chr9:33353720
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2730-366C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353720 | ||||||
| chr9:33353753
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2730-333A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353753 | ||||||
| chr9:33353923
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0139 | 4 | HG02155.hp1 NA18939.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2730-163C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | chr9 | 33353923 | ||||||
| chr9:33354072
|
TTTTTA | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(69): Show | 74 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
splice_region_variant&intron_variant | LOW | c.2730-12_2730-8delT others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr9 | 33354072 | |||||
| chr9:33354238
|
T | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2831+51T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 18/23 | chr9 | 33354238 | ||||||
| chr9:33354346
|
A | G | 1 | a0001c0001t0002g0227 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2831+159A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 18/23 | chr9 | 33354346 | ||||||
| chr9:33354590
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2832-261G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 18/23 | chr9 | 33354590 | ||||||
| chr9:33354594
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | NA18939.hp1 NA18952.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2832-257T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 18/23 | chr9 | 33354594 | ||||||
| chr9:33354724
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2832-127G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 18/23 | chr9 | 33354724 | ||||||
| chr9:33354939
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2873+47G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33354939 | ||||||
| chr9:33355431
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2873+539G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355431 | ||||||
| chr9:33355476
|
G | A | 34 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(31): Show | 34 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2873+584G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355476 | ||||||
| chr9:33355575
|
A | G | 5 | a0001c0001t0002g0242a0001c0001t0002g0266a0001c0001t0002g0267others(2): Show | 5 | HG00408.hp1 HG02155.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.2873+683A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355575 | ||||||
| chr9:33355641
|
C | CT | 6 | a0001c0001t0001g0036a0001c0001t0002g0228a0001c0001t0002g0241others(3): Show | 6 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2873+769dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33355641 | |||||
| chr9:33355641
|
CT | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 166 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.2873+769delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33355641 | |||||
| chr9:33355641
|
CTT | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(9): Show | 12 | HG01069.hp1 HG01243.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2873+768_2873+769d others(4): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33355641 | |||||
| chr9:33355737
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2873+845C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355737 | ||||||
| chr9:33355757
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2873+865G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355757 | ||||||
| chr9:33355763
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(19): Show | 24 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.2873+871G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355763 | ||||||
| chr9:33355937
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2873+1045G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33355937 | ||||||
| chr9:33356214
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2873+1322A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356214 | ||||||
| chr9:33356272
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2873+1380G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356272 | ||||||
| chr9:33356368
|
G | T | 19 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0201others(16): Show | 19 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2873+1476G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356368 | ||||||
| chr9:33356729
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01255.hp2 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2873+1837C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356729 | ||||||
| chr9:33356919
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2873+2027G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356919 | ||||||
| chr9:33356946
|
C | T | 3 | a0001c0001t0002g0254a0001c0001t0002g0265a0001c0001t0002g0287 | 3 | NA18973.hp2 NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2873+2054C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356946 | ||||||
| chr9:33356991
|
C | CA | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2873+2117dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33356991 | |||||
| chr9:33356991
|
C | G | 1 | a0001c0008t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2873+2099C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33356991 | ||||||
| chr9:33357010
|
T | A | 1 | a0001c0001t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2873+2118T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357010 | ||||||
| chr9:33357170
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2873+2278C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357170 | ||||||
| chr9:33357271
|
T | C | 3 | a0001c0001t0001g0257a0001c0001t0002g0238a0001c0001t0002g0260 | 3 | HG00609.hp2 NA18954.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2873+2379T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357271 | ||||||
| chr9:33357280
|
C | G | 3 | a0001c0001t0001g0257a0001c0001t0002g0238a0001c0001t0002g0260 | 3 | HG00609.hp2 NA18954.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2873+2388C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357280 | ||||||
| chr9:33357326
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2873+2434G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357326 | ||||||
| chr9:33357334
|
AAT | A | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2873+2455_2873+245 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33357334 | |||||
| chr9:33357411
|
T | C | 39 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(36): Show | 39 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2873+2519T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357411 | ||||||
| chr9:33357414
|
C | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0250 | 2 | NA18950.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2873+2522C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357414 | ||||||
| chr9:33357676
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2873+2784C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357676 | ||||||
| chr9:33357689
|
G | A | 1 | a0001c0003t0001g0183 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2873+2797G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357689 | ||||||
| chr9:33357705
|
C | CT | 11 | a0001c0001t0001g0025a0001c0001t0001g0045a0001c0001t0001g0153others(8): Show | 11 | HG01074.hp1 HG01256.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2873+2829dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33357705 | |||||
| chr9:33357709
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2873+2817T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357709 | ||||||
| chr9:33357746
|
A | G | 2 | a0001c0001t0002g0272a0001c0001t0002g0276 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2873+2854A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33357746 | ||||||
| chr9:33358066
|
C | T | 1 | a0001c0001t0001g0003 | 2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2873+3174C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358066 | ||||||
| chr9:33358121
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2873+3229T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358121 | ||||||
| chr9:33358135
|
T | C | 77 | a0001c0001t0001g0046a0001c0001t0001g0108a0001c0001t0001g0257others(74): Show | 78 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.2873+3243T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358135 | ||||||
| chr9:33358170
|
G | T | 2 | a0002c0002t0003g0171a0002c0002t0003g0172 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2873+3278G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358170 | ||||||
| chr9:33358209
|
C | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2873+3317C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358209 | ||||||
| chr9:33358343
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2873+3451C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358343 | ||||||
| chr9:33358401
|
G | A | 1 | a0001c0001t0007g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2873+3509G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358401 | ||||||
| chr9:33358511
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2873+3619A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358511 | ||||||
| chr9:33358525
|
T | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2873+3633T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358525 | ||||||
| chr9:33358633
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0070 | 2 | HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.2873+3741C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358633 | ||||||
| chr9:33358647
|
A | AT | 29 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0048others(26): Show | 29 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.2873+3788dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
A | ATT | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0165others(26): Show | 29 | HG00408.hp1 HG00639.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.2873+3787_2873+378 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
A | ATTT | 43 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(40): Show | 43 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.2873+3786_2873+378 others(7): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
A | ATTTT | 15 | a0001c0001t0001g0257a0001c0001t0002g0004a0001c0001t0002g0227others(12): Show | 16 | HG00609.hp2 HG00642.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2873+3785_2873+378 others(8): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
AT | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0037others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2873+3788delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
ATTTTTT | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2873+3783_2873+378 others(10): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
ATTTTTTT | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG02055.hp2 HG02071.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.2873+3782_2873+378 others(11): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358647
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2873+3775_2873+378 others(18): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33358647 | |||||
| chr9:33358947
|
C | T | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2873+4055C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33358947 | ||||||
| chr9:33359099
|
T | C | 35 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2873+4207T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359099 | ||||||
| chr9:33359355
|
T | G | 10 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0003g0171others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2873+4463T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359355 | ||||||
| chr9:33359361
|
G | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0039others(23): Show | 28 | HG00408.hp2 HG00438.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2873+4469G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359361 | ||||||
| chr9:33359370
|
G | A | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0006t0001g0177others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2873+4478G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359370 | ||||||
| chr9:33359551
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2874-4459A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359551 | ||||||
| chr9:33359577
|
C | T | 81 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(78): Show | 82 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2874-4433C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359577 | ||||||
| chr9:33359579
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2874-4431A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359579 | ||||||
| chr9:33359820
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2874-4190G>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33359820 | ||||||
| chr9:33360002
|
T | A | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2874-4008T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360002 | ||||||
| chr9:33360080
|
G | C | 1 | a0001c0001t0002g0263 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2874-3930G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360080 | ||||||
| chr9:33360081
|
T | A | 1 | a0002c0002t0003g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2874-3929T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360081 | ||||||
| chr9:33360127
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2874-3883A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360127 | ||||||
| chr9:33360184
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2874-3826G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360184 | ||||||
| chr9:33360293
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02717.hp2 HG02723.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874-3717G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360293 | ||||||
| chr9:33360596
|
C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG00408.hp2 HG00438.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874-3414C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360596 | ||||||
| chr9:33360649
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2874-3361G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360649 | ||||||
| chr9:33360677
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2874-3333C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360677 | ||||||
| chr9:33360991
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2874-3019C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33360991 | ||||||
| chr9:33361217
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2874-2793A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361217 | ||||||
| chr9:33361224
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2874-2786C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361224 | ||||||
| chr9:33361435
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2874-2575G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361435 | ||||||
| chr9:33361664
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2874-2346T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361664 | ||||||
| chr9:33361796
|
A | AAT | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG01255.hp2 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2874-2202_2874-220 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33361796 | |||||
| chr9:33361916
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2874-2094A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361916 | ||||||
| chr9:33361993
|
C | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01255.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2874-2017C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33361993 | ||||||
| chr9:33362101
|
A | T | 75 | a0001c0001t0001g0257a0001c0001t0002g0004a0001c0001t0002g0222others(72): Show | 76 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2874-1909A>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362101 | ||||||
| chr9:33362121
|
C | CA | 20 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0100others(17): Show | 20 | HG02083.hp1 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.2874-1873dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362121 | |||||
| chr9:33362338
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2874-1672C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362338 | ||||||
| chr9:33362399
|
G | A | 7 | a0001c0001t0001g0048a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.2874-1611G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362399 | ||||||
| chr9:33362470
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA18960.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2874-1540A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362470 | ||||||
| chr9:33362530
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2874-1480A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362530 | ||||||
| chr9:33362623
|
A | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 139 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.2874-1387A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362623 | ||||||
| chr9:33362630
|
T | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 295 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.2874-1380T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362630 | ||||||
| chr9:33362670
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2874-1340A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362670 | ||||||
| chr9:33362692
|
G | GT | 83 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(80): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2874-1290dupT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362692 | |||||
| chr9:33362692
|
G | GTT | 7 | a0001c0001t0001g0044a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01081.hp1 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2874-1291_2874-129 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362692 | |||||
| chr9:33362692
|
GT | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0013others(30): Show | 33 | HG01109.hp1 HG01123.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.2874-1290delT | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362692 | |||||
| chr9:33362692
|
GTT | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0162others(11): Show | 14 | HG01243.hp1 HG01255.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2874-1291_2874-129 others(6): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362692 | |||||
| chr9:33362692
|
GTTT | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0164a0001c0001t0001g0182others(3): Show | 6 | HG02615.hp2 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874-1292_2874-129 others(7): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33362692 | |||||
| chr9:33362797
|
G | A | 10 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0003g0171others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2874-1213G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362797 | ||||||
| chr9:33362806
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2874-1204C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362806 | ||||||
| chr9:33362807
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2874-1203G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362807 | ||||||
| chr9:33362821
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2874-1189A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33362821 | ||||||
| chr9:33363066
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2874-944A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33363066 | ||||||
| chr9:33363140
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2874-870G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33363140 | ||||||
| chr9:33363263
|
G | GTAT | 16 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0045others(13): Show | 16 | HG00280.hp1 HG01123.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.2874-712_2874-710d others(5): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
G | GTATTAT | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG01109.hp1 HG01361.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.2874-715_2874-710d others(8): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
G | GTATTATT others(2): Show |
7 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0004g0169others(4): Show | 7 | HG00639.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2874-718_2874-710d others(11): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
G | GTATTATT others(5): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0193 | 3 | HG02572.hp2 NA18960.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2874-721_2874-710d others(14): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
GTAT | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 22 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2874-712_2874-710d others(5): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
GTATTAT | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0186a0001c0001t0001g0192others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2874-715_2874-710d others(8): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363263
|
GTATTATT others(5): Show |
G | 81 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(78): Show | 82 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2874-721_2874-710d others(14): Show |
NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr9 | 33363263 | |||||
| chr9:33363565
|
T | G | 33 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(30): Show | 33 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2874-445T>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33363565 | ||||||
| chr9:33363945
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.2874-65C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 19/23 | chr9 | 33363945 | ||||||
| chr9:33364127
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2972+19G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 20/23 | chr9 | 33364127 | ||||||
| chr9:33364442
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2973-266G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 20/23 | chr9 | 33364442 | ||||||
| chr9:33364494
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2973-214T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 20/23 | chr9 | 33364494 | ||||||
| chr9:33364597
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2973-111G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 20/23 | chr9 | 33364597 | ||||||
| chr9:33364849
|
G | A | 2 | a0001c0001t0002g0227a0001c0001t0002g0295 | 2 | NA19007.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3039+75G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33364849 | ||||||
| chr9:33364912
|
T | C | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0173others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3039+138T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33364912 | ||||||
| chr9:33364935
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3039+161C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33364935 | ||||||
| chr9:33365126
|
T | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG02257.hp2 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3039+352T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365126 | ||||||
| chr9:33365157
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3039+383C>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365157 | ||||||
| chr9:33365290
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0080others(1): Show | 4 | HG02015.hp1 NA19001.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3039+516A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365290 | ||||||
| chr9:33365358
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3039+584C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365358 | ||||||
| chr9:33365565
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.3039+791G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365565 | ||||||
| chr9:33365906
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3040-723C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33365906 | ||||||
| chr9:33366234
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3040-395C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33366234 | ||||||
| chr9:33366400
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.3040-229C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 21/23 | chr9 | 33366400 | ||||||
| chr9:33366790
|
C | T | 1 | a0001c0008t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3185+16C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33366790 | ||||||
| chr9:33366823
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3185+49G>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33366823 | ||||||
| chr9:33367090
|
C | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(55): Show | 60 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.3185+316C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33367090 | ||||||
| chr9:33367110
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3185+336C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33367110 | ||||||
| chr9:33367170
|
G | A | 19 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0201others(16): Show | 19 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3186-345G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33367170 | ||||||
| chr9:33367411
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0014 | 2 | NA19001.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3186-104C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 22/23 | chr9 | 33367411 | ||||||
| chr9:33367766
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3290+147G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33367766 | ||||||
| chr9:33367981
|
C | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3290+362C>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33367981 | ||||||
| chr9:33368021
|
G | A | 3 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0174 | 3 | HG01884.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3290+402G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33368021 | ||||||
| chr9:33368236
|
C | CA | 17 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0257others(14): Show | 17 | HG00408.hp1 HG00609.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.3290+627dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr9 | 33368236 | |||||
| chr9:33368249
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3290+630A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33368249 | ||||||
| chr9:33368362
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3290+743T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33368362 | ||||||
| chr9:33368650
|
T | A | 35 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.3290+1031T>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33368650 | ||||||
| chr9:33368867
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3291-1039C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33368867 | ||||||
| chr9:33369074
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3291-832C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369074 | ||||||
| chr9:33369127
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3291-779G>A | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369127 | ||||||
| chr9:33369214
|
T | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0044others(18): Show | 23 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.3291-692T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369214 | ||||||
| chr9:33369352
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0135 | 2 | HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3291-554C>T | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369352 | ||||||
| chr9:33369353
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0135 | 2 | HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3291-553A>G | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369353 | ||||||
| chr9:33369358
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0135 | 2 | HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3291-548T>C | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | chr9 | 33369358 | ||||||
| chr9:33369736
|
T | TA | 4 | a0001c0001t0001g0044a0001c0001t0001g0071a0001c0001t0001g0094others(1): Show | 4 | HG02080.hp2 HG02083.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.3291-163dupA | NFX1 | ENSG00000086102.19 | transcript | ENST00000379540.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr9 | 33369736 |