Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4784 |
|---|---|
| ensemblid | ENSG00000008441.19 |
| hgncid | 7788 |
| symbol | NFIX |
| name | nuclear factor I X |
| refseq_nuc | NM_001365902.3 |
| refseq_prot | NP_001352831.1 |
| ensembl_nuc | ENST00000592199.6 |
| ensembl_prot | ENSP00000467512.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 12995475 |
| end | 13098796 |
| strand | + |
| ver | v1.2 |
| region | chr19:12995475-13098796 |
| region5000 | chr19:12990475-13103796 |
| regionname0 | NFIX_chr19_12995475_13098796 |
| regionname5000 | NFIX_chr19_12990475_13103796 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 502 | 252 | 80 | 64 | 62 | 6 | 38 | 38 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4511 | 165 | 37 | 43 | 51 | 4 | 28 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0002 | 0/0 | 4512 | 14 | 1 | 5 | 3 | 0 | 5 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0003 | 0/0 | 4510 | 14 | 13 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0004 | 0/0 | 4511 | 8 | 0 | 5 | 0 | 2 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0005 | 0/0 | 4511 | 6 | 5 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0006 | 0/0 | 4511 | 4 | 4 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0007 | 0/0 | 4512 | 3 | 0 | 0 | 3 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0008 | 0/0 | 4512 | 3 | 1 | 0 | 2 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0009 | 0/0 | 4511 | 3 | 3 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0010 | 0/0 | 4513 | 2 | 0 | 0 | 1 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0011 | 0/0 | 4510 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0012 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0013 | 0/0 | 4512 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0014 | 0/0 | 4511 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0015 | 0/0 | 4511 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0016 | 0/0 | 4511 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0017 | 0/0 | 4511 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0018 | 0/0 | 4511 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0019 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0020 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0021 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0022 | 0/0 | 4511 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0023 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0024 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0025 | 0/0 | 4511 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0026 | 0/0 | 4511 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0027 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0028 | 0/0 | 4511 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0029 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0030 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0031 | 0/0 | 4510 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0032 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0033 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0034 | 0/0 | 4511 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0035 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| t0036 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1509 | 250 | 80 | 64 | 62 | 6 | 36 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0002 | 0/0 | 1509 | 2 | 0 | 0 | 0 | 0 | 2 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6019 | 163 | 37 | 43 | 51 | 4 | 26 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0002 | 0/0 | 6020 | 14 | 1 | 5 | 3 | 0 | 5 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0003 | 0/0 | 6018 | 14 | 13 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0004 | 0/0 | 6019 | 8 | 0 | 5 | 0 | 2 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0005 | 0/0 | 6019 | 6 | 5 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0006 | 0/0 | 6019 | 4 | 4 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0007 | 0/0 | 6020 | 3 | 0 | 0 | 3 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0008 | 0/0 | 6020 | 3 | 1 | 0 | 2 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0009 | 0/0 | 6019 | 3 | 3 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0010 | 0/0 | 6021 | 2 | 0 | 0 | 1 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0011 | 0/0 | 6018 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0012 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0013 | 0/0 | 6020 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0014 | 0/0 | 6019 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0015 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0016 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0017 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0018 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0019 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0020 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0021 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0022 | 0/0 | 6019 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0023 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0024 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0025 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0026 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0027 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0028 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0029 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0030 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0031 | 0/0 | 6018 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0032 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0033 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0034 | 0/0 | 6019 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0035 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0001t0036 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| a0001c0002t0001 | 0/0 | 6019 | 2 | 0 | 0 | 0 | 0 | 2 | NFIX_chr19_12990475_13103796 | NFIX | copy fasta | chr19 | 12990475 | 13103796 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0011g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0013g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0015g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0017g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0018g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0019g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0020g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0023g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0024g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0025g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0026g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0027g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0028g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0029g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0030g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0031g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0032g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0033g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0034g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0035g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0036g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0105 | EUR | GBR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0094 | EUR | FIN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00639 | hp2 | a0001 | c0001 | t0013 | g0231 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0227 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0251 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0252 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01346 | hp2 | a0001 | c0001 | t0026 | g0046 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01433 | hp2 | a0001 | c0001 | t0028 | g0195 | AMR | CLM | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01934 | hp2 | a0001 | c0001 | t0031 | g0234 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01952 | hp2 | a0001 | c0001 | t0018 | g0183 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01981 | hp1 | a0001 | c0001 | t0025 | g0114 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0214 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02622 | hp1 | a0001 | c0001 | t0036 | g0011 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02922 | hp2 | a0001 | c0001 | t0035 | g0180 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02965 | hp1 | a0001 | c0001 | t0033 | g0069 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02970 | hp1 | a0001 | c0001 | t0027 | g0170 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0172 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0171 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0211 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03579 | hp2 | a0001 | c0001 | t0032 | g0157 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03688 | hp2 | a0001 | c0001 | t0017 | g0160 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0117 | SAS | PJL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0229 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03942 | hp2 | a0001 | c0001 | t0015 | g0132 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18906 | hp1 | a0001 | c0001 | t0030 | g0169 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0209 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18994 | hp2 | a0001 | c0001 | t0034 | g0020 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19007 | hp1 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19010 | hp2 | a0001 | c0001 | t0022 | g0088 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0237 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0244 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0238 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0236 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | YRI | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | ASW | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | GIH | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02109 | hp1 | a0001 | c0001 | t0029 | g0116 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ACB | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG03471 | hp2 | a0001 | c0001 | t0024 | g0119 | AFR | MSL | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | USA | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | USA | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA21309 | hp1 | a0001 | c0001 | t0023 | g0173 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0241 | REF | REF | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0204 | REF | REF | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:13081837
|
G | A | 1 | a0001c0002 | 2 | HG03654.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1236G>A | p.Ser412Ser | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/11 | 1599/6019 | 1236/1509 | 412/502 | chr19 | 13081837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12995747
|
C | T | 1 | a0001c0001t0036 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/11 | chr19 | 12995747 | ||||||
| chr19:12995766
|
G | A | 1 | a0001c0001t0015 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/11 | 72 | chr19 | 12995766 | |||||
| chr19:13094755
|
G | A | 1 | a0001c0001t0016 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 106 | chr19 | 13094755 | |||||
| chr19:13094888
|
G | A | 1 | a0001c0001t0017 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 239 | chr19 | 13094888 | |||||
| chr19:13094934
|
C | T | 1 | a0001c0001t0035 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*285C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 285 | chr19 | 13094934 | |||||
| chr19:13094981
|
C | A | 2 | a0001c0001t0005a0001c0001t0018 | 7 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*332C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 332 | chr19 | 13094981 | |||||
| chr19:13095208
|
T | C | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG03195.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*559T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 559 | chr19 | 13095208 | |||||
| chr19:13095253
|
G | A | 1 | a0001c0001t0021 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 604 | chr19 | 13095253 | |||||
| chr19:13095371
|
A | C | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 722 | chr19 | 13095371 | |||||
| chr19:13095372
|
C | A | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 723 | chr19 | 13095372 | |||||
| chr19:13095401
|
C | T | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*752C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 752 | chr19 | 13095401 | |||||
| chr19:13095409
|
C | A | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 760 | chr19 | 13095409 | |||||
| chr19:13095521
|
G | A | 1 | a0001c0001t0022 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 872 | chr19 | 13095521 | |||||
| chr19:13095837
|
C | T | 1 | a0001c0001t0013 | 2 | HG00639.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1188C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1188 | chr19 | 13095837 | |||||
| chr19:13096010
|
C | T | 1 | a0001c0001t0020 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1361C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1361 | chr19 | 13096010 | |||||
| chr19:13096069
|
C | T | 1 | a0001c0001t0033 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1420 | chr19 | 13096069 | |||||
| chr19:13096081
|
A | G | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1432A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1432 | chr19 | 13096081 | |||||
| chr19:13096211
|
T | C | 1 | a0001c0001t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1562T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1562 | chr19 | 13096211 | |||||
| chr19:13096211
|
TTCTC | T | 2 | a0001c0001t0012a0001c0001t0033 | 3 | HG02280.hp2 HG02896.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1568_*1571delCTCT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1568 | INFO_REALIGN_3_PRIME | chr19 | 13096211 | ||||
| chr19:13096332
|
G | C | 1 | a0001c0001t0004 | 8 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1683G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1683 | chr19 | 13096332 | |||||
| chr19:13096368
|
G | A | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1719G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1719 | chr19 | 13096368 | |||||
| chr19:13096417
|
C | G | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0018 | 11 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1768C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1768 | chr19 | 13096417 | |||||
| chr19:13096470
|
G | C | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(1): Show | 21 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1821G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1821 | chr19 | 13096470 | |||||
| chr19:13096493
|
G | C | 1 | a0001c0001t0024 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1844G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1844 | chr19 | 13096493 | |||||
| chr19:13096527
|
T | G | 1 | a0001c0001t0018 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 1878 | chr19 | 13096527 | |||||
| chr19:13096711
|
C | T | 1 | a0001c0001t0032 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2062C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2062 | chr19 | 13096711 | |||||
| chr19:13096874
|
T | G | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2225T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2225 | chr19 | 13096874 | |||||
| chr19:13096950
|
G | GA | 2 | a0001c0001t0008a0001c0001t0010 | 5 | HG03927.hp2 NA18962.hp1 NA18994.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2314dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2315 | INFO_REALIGN_3_PRIME | chr19 | 13096950 | ||||
| chr19:13096950
|
GA | G | 7 | a0001c0001t0003a0001c0001t0011a0001c0001t0019others(4): Show | 21 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2314delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2314 | INFO_REALIGN_3_PRIME | chr19 | 13096950 | ||||
| chr19:13096976
|
T | G | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2327 | chr19 | 13096976 | |||||
| chr19:13097059
|
G | GA | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(1): Show | 21 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2419dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2420 | INFO_REALIGN_3_PRIME | chr19 | 13097059 | ||||
| chr19:13097307
|
A | G | 1 | a0001c0001t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2658A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 2658 | chr19 | 13097307 | |||||
| chr19:13097651
|
G | A | 2 | a0001c0001t0011a0001c0001t0030 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3002G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3002 | chr19 | 13097651 | |||||
| chr19:13097723
|
C | T | 1 | a0001c0001t0028 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3074C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3074 | chr19 | 13097723 | |||||
| chr19:13097752
|
C | T | 1 | a0001c0001t0027 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3103C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3103 | chr19 | 13097752 | |||||
| chr19:13097863
|
C | T | 1 | a0001c0001t0011 | 2 | HG01192.hp2 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3214C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3214 | chr19 | 13097863 | |||||
| chr19:13097923
|
T | A | 1 | a0001c0001t0025 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3274 | chr19 | 13097923 | |||||
| chr19:13097926
|
C | T | 1 | a0001c0001t0009 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3277C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3277 | chr19 | 13097926 | |||||
| chr19:13097969
|
A | G | 1 | a0001c0001t0031 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3320A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3320 | chr19 | 13097969 | |||||
| chr19:13098213
|
C | A | 1 | a0001c0001t0026 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3564C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3564 | chr19 | 13098213 | |||||
| chr19:13098342
|
C | T | 1 | a0001c0001t0007 | 3 | NA19012.hp2 NA19064.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3693C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 11/11 | 3693 | chr19 | 13098342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12995977
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.27+113C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12995977 | ||||||
| chr19:12996068
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.27+204C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12996068 | ||||||
| chr19:12996142
|
C | CGT | 8 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0245others(5): Show | 8 | HG02622.hp2 HG02965.hp2 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+306_27+307dupTG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12996142 | |||||
| chr19:12996142
|
CGT | C | 151 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(148): Show | 151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.27+306_27+307delTG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12996142 | |||||
| chr19:12996142
|
CGTGT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+304_27+307delTG others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12996142 | |||||
| chr19:12996142
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.27+298_27+307delTG others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12996142 | |||||
| chr19:12996445
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27+581C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12996445 | ||||||
| chr19:12996552
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.27+688C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12996552 | ||||||
| chr19:12996782
|
C | G | 4 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163others(1): Show | 4 | HG01934.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+918C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12996782 | ||||||
| chr19:12997014
|
G | T | 28 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0239others(25): Show | 28 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.27+1150G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997014 | ||||||
| chr19:12997059
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+1195C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997059 | ||||||
| chr19:12997129
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.27+1265C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997129 | ||||||
| chr19:12997137
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.27+1273A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997137 | ||||||
| chr19:12997142
|
C | T | 2 | a0001c0001t0006g0243a0001c0001t0014g0217 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.27+1278C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997142 | ||||||
| chr19:12997150
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+1286A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997150 | ||||||
| chr19:12997157
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.27+1293T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997157 | ||||||
| chr19:12997277
|
A | G | 1 | a0001c0001t0032g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27+1413A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997277 | ||||||
| chr19:12997352
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.27+1488C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997352 | ||||||
| chr19:12997422
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.27+1558C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997422 | ||||||
| chr19:12997489
|
G | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02622.hp2 HG02965.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+1625G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997489 | ||||||
| chr19:12997520
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+1656C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997520 | ||||||
| chr19:12997722
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0017g0160 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.27+1858G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997722 | ||||||
| chr19:12997734
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.27+1870C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997734 | ||||||
| chr19:12997751
|
C | A | 1 | a0001c0002t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.27+1887C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997751 | ||||||
| chr19:12997808
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.27+1944T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997808 | ||||||
| chr19:12997986
|
T | C | 1 | a0001c0001t0034g0020 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.27+2122T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12997986 | ||||||
| chr19:12998183
|
C | A | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG03710.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.27+2319C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998183 | ||||||
| chr19:12998249
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+2385C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998249 | ||||||
| chr19:12998297
|
G | C | 1 | a0001c0001t0001g0021 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.27+2433G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998297 | ||||||
| chr19:12998324
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+2460C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998324 | ||||||
| chr19:12998370
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.27+2506C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998370 | ||||||
| chr19:12998433
|
A | T | 1 | a0001c0002t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.27+2569A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998433 | ||||||
| chr19:12998581
|
G | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+2717G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998581 | ||||||
| chr19:12998646
|
A | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.27+2782A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998646 | ||||||
| chr19:12998717
|
A | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.27+2853A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998717 | ||||||
| chr19:12998729
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+2865C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998729 | ||||||
| chr19:12998763
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2899G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998763 | ||||||
| chr19:12998789
|
A | C | 1 | a0001c0001t0006g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+2925A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998789 | ||||||
| chr19:12998884
|
C | G | 1 | a0001c0001t0006g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+3020C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998884 | ||||||
| chr19:12998887
|
G | C | 6 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0245others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+3023G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998887 | ||||||
| chr19:12998922
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+3058G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998922 | ||||||
| chr19:12998949
|
G | A | 36 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0087others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.27+3085G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998949 | ||||||
| chr19:12998969
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.27+3105G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998969 | ||||||
| chr19:12998989
|
A | T | 4 | a0001c0001t0003g0181a0001c0001t0003g0216a0001c0001t0006g0243others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3125A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12998989 | ||||||
| chr19:12999094
|
G | A | 85 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.27+3230G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999094 | ||||||
| chr19:12999141
|
C | T | 31 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0087others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.27+3277C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999141 | ||||||
| chr19:12999153
|
T | C | 1 | a0001c0001t0025g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.27+3289T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999153 | ||||||
| chr19:12999169
|
C | T | 4 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3305C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999169 | ||||||
| chr19:12999177
|
AT | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG00408.hp2 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+3327delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999177 | |||||
| chr19:12999212
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+3348C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999212 | ||||||
| chr19:12999318
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3454G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999318 | ||||||
| chr19:12999420
|
C | G | 1 | a0001c0001t0003g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+3556C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999420 | ||||||
| chr19:12999487
|
A | AAC | 3 | a0001c0001t0001g0024a0001c0001t0001g0113a0001c0001t0003g0085 | 3 | HG02735.hp2 HG02922.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+3651_27+3652dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999487 | |||||
| chr19:12999487
|
AAC | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0012g0212others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3651_27+3652del others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999487 | |||||
| chr19:12999487
|
AACAC | A | 60 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0029others(57): Show | 60 | HG00438.hp2 HG00741.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.27+3649_27+3652del others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999487 | |||||
| chr19:12999487
|
AACACAC | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.27+3647_27+3652del others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999487 | |||||
| chr19:12999487
|
AACACACA others(9): Show |
A | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.27+3637_27+3652del others(16): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 12999487 | |||||
| chr19:12999619
|
G | A | 4 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0014g0171others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3755G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999619 | ||||||
| chr19:12999640
|
CG | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(1): Show | 4 | HG00408.hp1 HG02056.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3777delG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999640 | ||||||
| chr19:12999792
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0007g0236a0001c0001t0007g0237others(1): Show | 4 | HG02273.hp1 NA19012.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3928C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999792 | ||||||
| chr19:12999840
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.27+3976T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 12999840 | ||||||
| chr19:13000028
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.27+4164C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000028 | ||||||
| chr19:13000028
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+4164C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000028 | ||||||
| chr19:13000041
|
C | T | 4 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0014g0171others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+4177C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000041 | ||||||
| chr19:13000145
|
T | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG01192.hp2 HG01243.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.27+4281T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000145 | ||||||
| chr19:13000152
|
G | A | 4 | a0001c0001t0003g0181a0001c0001t0003g0216a0001c0001t0006g0243others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+4288G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000152 | ||||||
| chr19:13000560
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+4696G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000560 | ||||||
| chr19:13000563
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.27+4699G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000563 | ||||||
| chr19:13000572
|
G | A | 21 | a0001c0001t0001g0239a0001c0001t0002g0159a0001c0001t0002g0219others(18): Show | 21 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.27+4708G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000572 | ||||||
| chr19:13000657
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+4793G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000657 | ||||||
| chr19:13000717
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.27+4853G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000717 | ||||||
| chr19:13000719
|
C | T | 4 | a0001c0001t0003g0181a0001c0001t0003g0216a0001c0001t0006g0243others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+4855C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000719 | ||||||
| chr19:13000759
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27+4895G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000759 | ||||||
| chr19:13000821
|
G | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG01192.hp2 HG01243.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.27+4957G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13000821 | ||||||
| chr19:13001276
|
C | T | 7 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+5412C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001276 | ||||||
| chr19:13001323
|
G | A | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+5459G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001323 | ||||||
| chr19:13001339
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.27+5475T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001339 | ||||||
| chr19:13001454
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0022others(7): Show | 10 | HG01433.hp2 HG01516.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+5590C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001454 | ||||||
| chr19:13001585
|
C | T | 1 | a0001c0001t0007g0238 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.27+5721C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001585 | ||||||
| chr19:13001698
|
A | G | 4 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0014g0171others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+5834A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001698 | ||||||
| chr19:13001722
|
G | A | 1 | a0001c0001t0024g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.27+5858G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001722 | ||||||
| chr19:13001754
|
G | A | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+5890G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001754 | ||||||
| chr19:13001917
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+6053G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13001917 | ||||||
| chr19:13002043
|
G | T | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+6179G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002043 | ||||||
| chr19:13002051
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.27+6187G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002051 | ||||||
| chr19:13002083
|
C | T | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+6219C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002083 | ||||||
| chr19:13002084
|
G | A | 1 | a0001c0001t0023g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+6220G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002084 | ||||||
| chr19:13002134
|
G | A | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+6270G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002134 | ||||||
| chr19:13002160
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27+6296C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002160 | ||||||
| chr19:13002250
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.27+6386C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002250 | ||||||
| chr19:13002398
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.27+6534C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002398 | ||||||
| chr19:13002471
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+6607G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002471 | ||||||
| chr19:13002606
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.27+6742C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002606 | ||||||
| chr19:13002735
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+6871G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002735 | ||||||
| chr19:13002780
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.27+6916C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002780 | ||||||
| chr19:13002827
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 164 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.27+6963T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002827 | ||||||
| chr19:13002917
|
G | C | 1 | a0001c0001t0006g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+7053G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002917 | ||||||
| chr19:13002964
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+7100G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002964 | ||||||
| chr19:13002982
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.27+7118A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13002982 | ||||||
| chr19:13003062
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+7198C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003062 | ||||||
| chr19:13003080
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.27+7216G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003080 | ||||||
| chr19:13003620
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.27+7756A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003620 | ||||||
| chr19:13003872
|
T | C | 1 | a0001c0001t0008g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.27+8008T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003872 | ||||||
| chr19:13003886
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.27+8022C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003886 | ||||||
| chr19:13003920
|
G | A | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG01243.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.27+8056G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13003920 | ||||||
| chr19:13004170
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27+8306C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004170 | ||||||
| chr19:13004174
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.27+8310G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004174 | ||||||
| chr19:13004356
|
T | A | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.27+8492T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004356 | ||||||
| chr19:13004454
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.27+8590C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004454 | ||||||
| chr19:13004495
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(22): Show | 25 | HG01192.hp2 HG01243.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.27+8631G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004495 | ||||||
| chr19:13004624
|
T | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+8760T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004624 | ||||||
| chr19:13004666
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG01192.hp2 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.27+8802G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004666 | ||||||
| chr19:13004724
|
C | T | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+8860C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004724 | ||||||
| chr19:13004820
|
C | CT | 12 | a0001c0001t0001g0084a0001c0001t0001g0111a0001c0001t0003g0081others(9): Show | 12 | HG01175.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.27+8973dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13004820 | |||||
| chr19:13004820
|
C | CTT | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+8972_27+8973dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13004820 | |||||
| chr19:13004881
|
A | G | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+9017A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004881 | ||||||
| chr19:13004915
|
C | G | 1 | a0001c0001t0011g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27+9051C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13004915 | ||||||
| chr19:13005231
|
G | A | 20 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220others(17): Show | 20 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+9367G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005231 | ||||||
| chr19:13005358
|
C | T | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.27+9494C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005358 | ||||||
| chr19:13005428
|
C | T | 85 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.27+9564C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005428 | ||||||
| chr19:13005622
|
G | A | 4 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0014g0171others(1): Show | 4 | HG01192.hp2 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+9758G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005622 | ||||||
| chr19:13005639
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.27+9775G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005639 | ||||||
| chr19:13005707
|
T | C | 87 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.27+9843T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005707 | ||||||
| chr19:13005722
|
A | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+9858A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005722 | ||||||
| chr19:13006100
|
G | A | 1 | a0001c0001t0016g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.27+10236G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006100 | ||||||
| chr19:13006201
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.27+10337G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006201 | ||||||
| chr19:13006213
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.27+10349G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006213 | ||||||
| chr19:13006225
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0005g0126a0001c0001t0027g0170 | 3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.27+10361A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006225 | ||||||
| chr19:13006259
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0020g0244 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.27+10395T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006259 | ||||||
| chr19:13006480
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | NA18966.hp2 NA18990.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.27+10616G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006480 | ||||||
| chr19:13006727
|
C | T | 1 | a0001c0001t0032g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27+10863C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13006727 | ||||||
| chr19:13007046
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.27+11182C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007046 | ||||||
| chr19:13007068
|
G | A | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.27+11204G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007068 | ||||||
| chr19:13007082
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.27+11218C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007082 | ||||||
| chr19:13007356
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.27+11492T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007356 | ||||||
| chr19:13007378
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+11514C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007378 | ||||||
| chr19:13007395
|
C | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0242 | 3 | HG02055.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+11531C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007395 | ||||||
| chr19:13007610
|
C | T | 1 | a0001c0001t0028g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.27+11746C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007610 | ||||||
| chr19:13007711
|
C | A | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.27+11847C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007711 | ||||||
| chr19:13007741
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+11877G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007741 | ||||||
| chr19:13007896
|
C | G | 3 | a0001c0001t0002g0235a0001c0001t0011g0251a0001c0001t0011g0252 | 3 | HG01192.hp2 HG01243.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.27+12032C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13007896 | ||||||
| chr19:13008054
|
A | G | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.27+12190A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008054 | ||||||
| chr19:13008105
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.27+12241C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008105 | ||||||
| chr19:13008142
|
T | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+12278T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008142 | ||||||
| chr19:13008289
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.27+12425A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008289 | ||||||
| chr19:13008455
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27+12591C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008455 | ||||||
| chr19:13008483
|
C | T | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.27+12619C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008483 | ||||||
| chr19:13008557
|
G | C | 3 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238 | 3 | NA19012.hp2 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.27+12693G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008557 | ||||||
| chr19:13008662
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0032g0157 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.27+12798G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008662 | ||||||
| chr19:13008718
|
C | T | 28 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0079others(25): Show | 28 | HG00639.hp1 HG00642.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.27+12854C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008718 | ||||||
| chr19:13008861
|
G | A | 7 | a0001c0001t0004g0017a0001c0001t0004g0091a0001c0001t0004g0092others(4): Show | 7 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+12997G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008861 | ||||||
| chr19:13008911
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.27+13047A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008911 | ||||||
| chr19:13008921
|
C | T | 1 | a0001c0001t0008g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27+13057C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13008921 | ||||||
| chr19:13009175
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.27+13311A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13009175 | ||||||
| chr19:13009320
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02004.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.27+13456G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13009320 | ||||||
| chr19:13009327
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.27+13463C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13009327 | ||||||
| chr19:13010025
|
C | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+14161C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010025 | ||||||
| chr19:13010030
|
G | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+14166G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010030 | ||||||
| chr19:13010100
|
T | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.27+14236T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010100 | ||||||
| chr19:13010112
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.27+14248C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010112 | ||||||
| chr19:13010228
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0005g0120others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+14364C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010228 | ||||||
| chr19:13010339
|
G | T | 3 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.27+14475G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010339 | ||||||
| chr19:13010654
|
T | C | 1 | a0001c0001t0027g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.28-14367T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010654 | ||||||
| chr19:13010670
|
G | T | 3 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.28-14351G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010670 | ||||||
| chr19:13010671
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.28-14350C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010671 | ||||||
| chr19:13010672
|
T | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.28-14349T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010672 | ||||||
| chr19:13010913
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-14108C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13010913 | ||||||
| chr19:13011025
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-13996C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011025 | ||||||
| chr19:13011025
|
C | G | 1 | a0001c0001t0007g0237 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.28-13996C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011025 | ||||||
| chr19:13011047
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.28-13974A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011047 | ||||||
| chr19:13011119
|
G | C | 3 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238 | 3 | NA19012.hp2 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.28-13902G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011119 | ||||||
| chr19:13011182
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.28-13839G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011182 | ||||||
| chr19:13011375
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-13646C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011375 | ||||||
| chr19:13011410
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.28-13611T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011410 | ||||||
| chr19:13011485
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.28-13536C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011485 | ||||||
| chr19:13011554
|
G | A | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-13467G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011554 | ||||||
| chr19:13011798
|
A | G | 109 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.28-13223A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011798 | ||||||
| chr19:13011878
|
G | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-13143G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011878 | ||||||
| chr19:13011880
|
G | C | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.28-13141G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011880 | ||||||
| chr19:13011884
|
A | AC | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-13137_28-13136i others(3): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011884 | ||||||
| chr19:13011968
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28-13053C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13011968 | ||||||
| chr19:13012003
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.28-13018C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012003 | ||||||
| chr19:13012374
|
C | T | 51 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0086others(48): Show | 51 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.28-12647C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012374 | ||||||
| chr19:13012438
|
C | T | 2 | a0001c0001t0008g0201a0001c0001t0008g0209 | 2 | NA18962.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.28-12583C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012438 | ||||||
| chr19:13012699
|
G | A | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.28-12322G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012699 | ||||||
| chr19:13012933
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28-12088T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012933 | ||||||
| chr19:13012936
|
AG | A | 32 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0087others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-12082delG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13012936 | |||||
| chr19:13012947
|
G | C | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-12074G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13012947 | ||||||
| chr19:13013017
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.28-12004C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013017 | ||||||
| chr19:13013056
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.28-11965G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013056 | ||||||
| chr19:13013064
|
T | TA | 25 | a0001c0001t0001g0032a0001c0001t0001g0068a0001c0001t0001g0070others(22): Show | 25 | HG00738.hp1 HG01934.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.28-11947dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13013064 | |||||
| chr19:13013064
|
T | TAA | 73 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(70): Show | 73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.28-11948_28-11947d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13013064 | |||||
| chr19:13013088
|
A | C | 13 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0222others(10): Show | 13 | HG01109.hp2 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-11933A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013088 | ||||||
| chr19:13013373
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.28-11648C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013373 | ||||||
| chr19:13013612
|
T | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-11409T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013612 | ||||||
| chr19:13013649
|
A | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.28-11372A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13013649 | ||||||
| chr19:13013686
|
C | CT | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-11325dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13013686 | |||||
| chr19:13014306
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.28-10715C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014306 | ||||||
| chr19:13014316
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.28-10705C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014316 | ||||||
| chr19:13014429
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0003g0174 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.28-10592G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014429 | ||||||
| chr19:13014624
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.28-10397A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014624 | ||||||
| chr19:13014860
|
TGGGCTGG others(7): Show |
T | 1 | a0001c0001t0005g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.28-10146_28-10133d others(16): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13014860 | |||||
| chr19:13014906
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-10115C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014906 | ||||||
| chr19:13014961
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0154 | 3 | HG02895.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.28-10060C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014961 | ||||||
| chr19:13014979
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.28-10042A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13014979 | ||||||
| chr19:13015083
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.28-9938T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015083 | ||||||
| chr19:13015160
|
C | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.28-9861C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015160 | ||||||
| chr19:13015513
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28-9508A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015513 | ||||||
| chr19:13015790
|
T | TCA | 12 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(9): Show | 12 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-9209_28-9208dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13015790 | |||||
| chr19:13015790
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0031g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.28-9217_28-9208del others(10): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13015790 | |||||
| chr19:13015794
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-9227A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015794 | ||||||
| chr19:13015808
|
A | ACACACAC others(1): Show |
5 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0043others(2): Show | 5 | HG00438.hp1 HG02165.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-9208_28-9207ins others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13015808 | |||||
| chr19:13015808
|
A | ACACACG | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.28-9197_28-9192dup others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13015808 | |||||
| chr19:13015808
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0029g0116 | 2 | HG02109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.28-9213A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015808 | ||||||
| chr19:13015852
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.28-9169G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13015852 | ||||||
| chr19:13016129
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.28-8892C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016129 | ||||||
| chr19:13016243
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.28-8778G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016243 | ||||||
| chr19:13016403
|
AT | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-8614delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13016403 | |||||
| chr19:13016409
|
A | C | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-8612A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016409 | ||||||
| chr19:13016442
|
G | C | 1 | a0001c0001t0002g0128 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.28-8579G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016442 | ||||||
| chr19:13016654
|
GT | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0124a0001c0001t0003g0177others(9): Show | 12 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-8351delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13016654 | |||||
| chr19:13016760
|
G | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-8261G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016760 | ||||||
| chr19:13016801
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.28-8220G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016801 | ||||||
| chr19:13016814
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-8207G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13016814 | ||||||
| chr19:13017337
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp1 HG02293.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.28-7684G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017337 | ||||||
| chr19:13017356
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28-7665G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017356 | ||||||
| chr19:13017752
|
G | C | 1 | a0001c0001t0024g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-7269G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017752 | ||||||
| chr19:13017761
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.28-7260C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017761 | ||||||
| chr19:13017764
|
C | G | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-7257C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017764 | ||||||
| chr19:13017850
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.28-7171A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017850 | ||||||
| chr19:13017977
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.28-7044C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13017977 | ||||||
| chr19:13018047
|
G | A | 30 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(27): Show | 30 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.28-6974G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018047 | ||||||
| chr19:13018259
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-6762C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018259 | ||||||
| chr19:13018335
|
C | CG | 53 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.28-6670dupG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13018335 | |||||
| chr19:13018335
|
C | CGG | 40 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.28-6671_28-6670dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13018335 | |||||
| chr19:13018335
|
CG | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(47): Show | 50 | HG00438.hp1 HG01070.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-6670delG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13018335 | |||||
| chr19:13018335
|
CGG | C | 16 | a0001c0001t0001g0024a0001c0001t0001g0087a0001c0001t0001g0097others(13): Show | 16 | HG00738.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-6671_28-6670del others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13018335 | |||||
| chr19:13018336
|
G | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-6685G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018336 | ||||||
| chr19:13018339
|
G | A | 2 | a0001c0001t0003g0181a0001c0001t0003g0216 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-6682G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018339 | ||||||
| chr19:13018340
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-6681G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018340 | ||||||
| chr19:13018341
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-6680G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018341 | ||||||
| chr19:13018365
|
A | G | 1 | a0001c0001t0004g0095 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.28-6656A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018365 | ||||||
| chr19:13018659
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.28-6362A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018659 | ||||||
| chr19:13018740
|
A | G | 1 | a0001c0001t0003g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-6281A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13018740 | ||||||
| chr19:13019003
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28-6018T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019003 | ||||||
| chr19:13019118
|
A | AT | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.28-5890dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019118 | |||||
| chr19:13019182
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.28-5839T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019182 | ||||||
| chr19:13019370
|
T | C | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.28-5651T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019370 | ||||||
| chr19:13019440
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0215 | 2 | HG00639.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.28-5581C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019440 | ||||||
| chr19:13019712
|
GT | G | 81 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(78): Show | 81 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.28-5299delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019712 | |||||
| chr19:13019722
|
T | G | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-5299T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019722 | ||||||
| chr19:13019723
|
G | T | 4 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5298G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019723 | ||||||
| chr19:13019727
|
G | GT | 6 | a0001c0001t0001g0084a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG00741.hp1 HG02055.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5291dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019727 | |||||
| chr19:13019727
|
G | GTT | 3 | a0001c0001t0003g0177a0001c0001t0032g0157a0001c0001t0035g0180 | 3 | HG02922.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.28-5292_28-5291dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019727 | |||||
| chr19:13019727
|
G | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.28-5294G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019727 | ||||||
| chr19:13019729
|
TTG | T | 5 | a0001c0001t0001g0213a0001c0001t0001g0247a0001c0001t0012g0212others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5290_28-5289del others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019729 | |||||
| chr19:13019730
|
TG | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0152a0001c0001t0014g0171others(1): Show | 4 | HG02129.hp1 HG03098.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5290delG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019730 | ||||||
| chr19:13019731
|
G | GT | 9 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-5274dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019731 | |||||
| chr19:13019731
|
G | T | 23 | a0001c0001t0001g0084a0001c0001t0001g0129a0001c0001t0001g0130others(20): Show | 23 | HG00741.hp1 HG01934.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.28-5290G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019731 | ||||||
| chr19:13019731
|
GT | G | 30 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0065others(27): Show | 30 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.28-5274delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019731 | |||||
| chr19:13019735
|
T | G | 70 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.28-5286T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019735 | ||||||
| chr19:13019736
|
T | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0087 | 2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.28-5285T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019736 | ||||||
| chr19:13019737
|
T | G | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.28-5284T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019737 | ||||||
| chr19:13019738
|
T | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.28-5283T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019738 | ||||||
| chr19:13019773
|
A | G | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-5248A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13019773 | ||||||
| chr19:13019940
|
C | CT | 34 | a0001c0001t0001g0027a0001c0001t0001g0084a0001c0001t0001g0175others(31): Show | 34 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-5071dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13019940 | |||||
| chr19:13020040
|
C | T | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.28-4981C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13020040 | ||||||
| chr19:13020178
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.28-4843A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13020178 | ||||||
| chr19:13020332
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.28-4689A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13020332 | ||||||
| chr19:13020557
|
C | A | 1 | a0001c0001t0022g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.28-4464C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13020557 | ||||||
| chr19:13021401
|
G | T | 22 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(19): Show | 22 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.28-3620G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13021401 | ||||||
| chr19:13021680
|
A | C | 18 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.28-3341A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13021680 | ||||||
| chr19:13021973
|
C | T | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.28-3048C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13021973 | ||||||
| chr19:13022341
|
G | A | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.28-2680G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13022341 | ||||||
| chr19:13023028
|
C | T | 1 | a0001c0001t0006g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1993C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023028 | ||||||
| chr19:13023030
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.28-1991T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023030 | ||||||
| chr19:13023070
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.28-1951T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023070 | ||||||
| chr19:13023070
|
T | TCTCTCTC others(12): Show |
1 | a0001c0001t0003g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.28-1951_28-1950ins others(19): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023070 | ||||||
| chr19:13023070
|
T | TTC | 81 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.28-1925_28-1924dup others(2): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTC | 8 | a0001c0001t0001g0025a0001c0001t0001g0065a0001c0001t0001g0067others(5): Show | 8 | HG02056.hp1 HG02132.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1927_28-1924dup others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTC | 100 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0024others(97): Show | 100 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.28-1929_28-1924dup others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(1): Show |
10 | a0001c0001t0001g0076a0001c0001t0003g0085a0001c0001t0003g0162others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-1931_28-1924dup others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(3): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0247a0001c0001t0002g0228 | 3 | HG02040.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.28-1933_28-1924dup others(10): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(5): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(14): Show | 17 | HG01192.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-1935_28-1924dup others(12): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(9): Show |
6 | a0001c0001t0001g0213a0001c0001t0009g0010a0001c0001t0011g0252others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1939_28-1924dup others(16): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(11): Show |
14 | a0001c0001t0001g0124a0001c0001t0003g0181a0001c0001t0005g0120others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-1941_28-1924dup others(18): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(13): Show |
2 | a0001c0001t0003g0216a0001c0001t0009g0007 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-1943_28-1924dup others(20): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023070
|
T | TTCTCTCT others(15): Show |
1 | a0001c0001t0029g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.28-1945_28-1924dup others(22): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023070 | |||||
| chr19:13023204
|
C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0112others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-1805dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023204 | |||||
| chr19:13023237
|
T | G | 1 | a0001c0001t0006g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-1784T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023237 | ||||||
| chr19:13023630
|
CT | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0178others(5): Show | 8 | HG02273.hp1 HG02897.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-1376delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023630 | |||||
| chr19:13023630
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(19): Show | 22 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.28-1383_28-1376del others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13023630 | |||||
| chr19:13023687
|
A | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0146a0001c0001t0001g0165others(2): Show | 5 | HG00408.hp1 HG00438.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-1334A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023687 | ||||||
| chr19:13023828
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.28-1193G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13023828 | ||||||
| chr19:13024000
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-1021G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024000 | ||||||
| chr19:13024113
|
C | CA | 24 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0057others(21): Show | 24 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.28-891dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13024113 | |||||
| chr19:13024113
|
CA | C | 10 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0109others(7): Show | 10 | HG00323.hp2 HG02165.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-891delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 13024113 | |||||
| chr19:13024194
|
G | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-827G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024194 | ||||||
| chr19:13024219
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.28-802G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024219 | ||||||
| chr19:13024383
|
T | C | 32 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(29): Show | 32 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-638T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024383 | ||||||
| chr19:13024410
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.28-611G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024410 | ||||||
| chr19:13024548
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.28-473C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024548 | ||||||
| chr19:13024744
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.28-277G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13024744 | ||||||
| chr19:13025878
|
G | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+326G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13025878 | ||||||
| chr19:13026016
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.559+464C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026016 | ||||||
| chr19:13026017
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.559+465G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026017 | ||||||
| chr19:13026033
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0003g0174 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.559+481C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026033 | ||||||
| chr19:13026250
|
A | C | 1 | a0001c0001t0025g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.559+698A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026250 | ||||||
| chr19:13026380
|
C | CA | 6 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0190others(3): Show | 6 | HG01433.hp1 HG01934.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+842dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13026380 | |||||
| chr19:13026447
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.559+895G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026447 | ||||||
| chr19:13026543
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.559+991T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026543 | ||||||
| chr19:13026724
|
T | TTCTC | 97 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.559+1190_559+1193d others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13026724 | |||||
| chr19:13026724
|
T | TTCTCTC | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+1188_559+1193d others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13026724 | |||||
| chr19:13026744
|
C | CTG | 24 | a0001c0001t0001g0075a0001c0001t0001g0176a0001c0001t0002g0128others(21): Show | 24 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.559+1216_559+1217d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13026744 | |||||
| chr19:13026744
|
C | CTGTG | 8 | a0001c0001t0001g0084a0001c0001t0001g0247a0001c0001t0003g0081others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+1214_559+1217d others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13026744 | |||||
| chr19:13026744
|
C | G | 5 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(2): Show | 5 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+1192C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026744 | ||||||
| chr19:13026746
|
G | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 103 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.559+1194G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026746 | ||||||
| chr19:13026748
|
G | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0008g0006others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1196G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026748 | ||||||
| chr19:13026750
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.559+1198G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026750 | ||||||
| chr19:13026752
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.559+1200G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026752 | ||||||
| chr19:13026754
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.559+1202G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026754 | ||||||
| chr19:13026828
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1276C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026828 | ||||||
| chr19:13026910
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.559+1358G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13026910 | ||||||
| chr19:13027059
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+1507C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027059 | ||||||
| chr19:13027077
|
T | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+1525T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027077 | ||||||
| chr19:13027182
|
C | A | 1 | a0001c0001t0008g0209 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.559+1630C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027182 | ||||||
| chr19:13027543
|
T | C | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.559+1991T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027543 | ||||||
| chr19:13027588
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+2036C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027588 | ||||||
| chr19:13027761
|
A | G | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG01243.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.559+2209A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027761 | ||||||
| chr19:13027768
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02132.hp2 NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.559+2216G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027768 | ||||||
| chr19:13027841
|
G | A | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.559+2289G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13027841 | ||||||
| chr19:13028416
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.559+2864G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028416 | ||||||
| chr19:13028666
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.559+3114G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028666 | ||||||
| chr19:13028802
|
A | G | 22 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(19): Show | 22 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+3250A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028802 | ||||||
| chr19:13028845
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.559+3293C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028845 | ||||||
| chr19:13028846
|
G | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+3294G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028846 | ||||||
| chr19:13028942
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0003g0174 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.559+3390A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028942 | ||||||
| chr19:13028976
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.559+3424G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13028976 | ||||||
| chr19:13029018
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.559+3466G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029018 | ||||||
| chr19:13029527
|
T | C | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.559+3975T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029527 | ||||||
| chr19:13029580
|
G | A | 1 | a0001c0001t0019g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.559+4028G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029580 | ||||||
| chr19:13029598
|
C | A | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.559+4046C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029598 | ||||||
| chr19:13029733
|
A | G | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+4181A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029733 | ||||||
| chr19:13029816
|
T | C | 1 | a0001c0001t0018g0183 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.559+4264T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13029816 | ||||||
| chr19:13030182
|
C | T | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.559+4630C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13030182 | ||||||
| chr19:13030599
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.559+5047C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13030599 | ||||||
| chr19:13030628
|
TGGCTCCT others(1): Show |
T | 7 | a0001c0001t0001g0124a0001c0001t0005g0120a0001c0001t0005g0121others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+5078_559+5085d others(10): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13030628 | |||||
| chr19:13030844
|
G | A | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.559+5292G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13030844 | ||||||
| chr19:13030906
|
G | T | 1 | a0001c0001t0007g0237 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.559+5354G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13030906 | ||||||
| chr19:13030908
|
G | A | 5 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(2): Show | 5 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+5356G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13030908 | ||||||
| chr19:13031050
|
G | C | 10 | a0001c0001t0001g0213a0001c0001t0006g0168a0001c0001t0006g0182others(7): Show | 10 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+5498G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031050 | ||||||
| chr19:13031306
|
G | A | 2 | a0001c0001t0006g0153a0001c0001t0019g0211 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.559+5754G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031306 | ||||||
| chr19:13031452
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.559+5900C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031452 | ||||||
| chr19:13031495
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.559+5943A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031495 | ||||||
| chr19:13031650
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0192 | 3 | HG02129.hp2 HG02132.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.559+6098G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031650 | ||||||
| chr19:13031833
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+6281C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13031833 | ||||||
| chr19:13032423
|
G | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+6871G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032423 | ||||||
| chr19:13032441
|
A | G | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+6889A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032441 | ||||||
| chr19:13032490
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.559+6938G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032490 | ||||||
| chr19:13032581
|
T | C | 20 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(17): Show | 20 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.559+7029T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032581 | ||||||
| chr19:13032874
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+7322C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032874 | ||||||
| chr19:13032912
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.559+7360G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032912 | ||||||
| chr19:13032977
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.559+7425C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13032977 | ||||||
| chr19:13033248
|
A | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.559+7696A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13033248 | ||||||
| chr19:13033763
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.559+8211T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13033763 | ||||||
| chr19:13033776
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+8224T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13033776 | ||||||
| chr19:13034127
|
G | A | 1 | a0001c0001t0025g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.559+8575G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034127 | ||||||
| chr19:13034135
|
G | A | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+8583G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034135 | ||||||
| chr19:13034306
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.559+8754C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034306 | ||||||
| chr19:13034385
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.559+8833G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034385 | ||||||
| chr19:13034400
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0215 | 2 | HG00639.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.559+8848G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034400 | ||||||
| chr19:13034429
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.559+8877G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034429 | ||||||
| chr19:13034664
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.559+9112G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034664 | ||||||
| chr19:13034854
|
T | TG | 34 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(31): Show | 34 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.559+9303dupG | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13034854 | |||||
| chr19:13034856
|
A | C | 34 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(31): Show | 34 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.559+9304A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034856 | ||||||
| chr19:13034993
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0041others(5): Show | 8 | HG00408.hp2 HG00673.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+9441C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13034993 | ||||||
| chr19:13035464
|
G | C | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.559+9912G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13035464 | ||||||
| chr19:13035522
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+9970C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13035522 | ||||||
| chr19:13035525
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.559+9973T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13035525 | ||||||
| chr19:13035846
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.559+10294T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13035846 | ||||||
| chr19:13035891
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+10339C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13035891 | ||||||
| chr19:13036286
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0026g0046 | 2 | HG00323.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.559+10734G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13036286 | ||||||
| chr19:13036454
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.559+10902C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13036454 | ||||||
| chr19:13036566
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0012g0214 | 2 | HG01943.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.559+11014C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13036566 | ||||||
| chr19:13037100
|
C | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+11548C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037100 | ||||||
| chr19:13037239
|
C | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+11687C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037239 | ||||||
| chr19:13037292
|
G | A | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.559+11740G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037292 | ||||||
| chr19:13037295
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.559+11743T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037295 | ||||||
| chr19:13037337
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0107others(1): Show | 4 | HG01255.hp2 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+11785C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037337 | ||||||
| chr19:13037452
|
G | A | 1 | a0001c0001t0004g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.559+11900G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037452 | ||||||
| chr19:13037551
|
G | C | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.559+11999G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037551 | ||||||
| chr19:13037687
|
C | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0074 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.559+12135C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037687 | ||||||
| chr19:13037700
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.559+12148G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037700 | ||||||
| chr19:13037761
|
G | A | 45 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0115others(42): Show | 45 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.559+12209G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037761 | ||||||
| chr19:13037856
|
A | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0056others(4): Show | 7 | HG00735.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+12304A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037856 | ||||||
| chr19:13037891
|
C | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.559+12339C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037891 | ||||||
| chr19:13037902
|
C | G | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.559+12350C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13037902 | ||||||
| chr19:13038132
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.559+12580T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13038132 | ||||||
| chr19:13038516
|
A | G | 1 | a0001c0001t0004g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.559+12964A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13038516 | ||||||
| chr19:13038554
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0002t0001g0019others(1): Show | 4 | HG03654.hp2 HG03834.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+13002A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13038554 | ||||||
| chr19:13038805
|
G | A | 1 | a0001c0001t0014g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.559+13253G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13038805 | ||||||
| chr19:13039040
|
T | C | 10 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+13488T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039040 | ||||||
| chr19:13039050
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.559+13498A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039050 | ||||||
| chr19:13039221
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.559+13669C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039221 | ||||||
| chr19:13039228
|
C | A | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.559+13676C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039228 | ||||||
| chr19:13039228
|
C | CA | 4 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+13676_559+1367 others(5): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039228 | ||||||
| chr19:13039229
|
CA | C | 7 | a0001c0001t0001g0124a0001c0001t0005g0120a0001c0001t0005g0121others(4): Show | 7 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+13678delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039229 | ||||||
| chr19:13039230
|
A | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG01934.hp1 HG02258.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.559+13678A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039230 | ||||||
| chr19:13039232
|
A | C | 1 | a0001c0001t0021g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559+13680A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039232 | ||||||
| chr19:13039241
|
T | C | 34 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(31): Show | 34 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.559+13689T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039241 | ||||||
| chr19:13039244
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0161 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559+13692A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039244 | ||||||
| chr19:13039245
|
C | CACACGT | 3 | a0001c0001t0001g0176a0001c0001t0003g0162a0001c0001t0017g0160 | 3 | HG01934.hp1 HG02630.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.559+13693_559+1369 others(10): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039245 | ||||||
| chr19:13039245
|
C | CACGT | 6 | a0001c0001t0003g0150a0001c0001t0003g0164a0001c0001t0003g0177others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+13693_559+1369 others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039245 | ||||||
| chr19:13039245
|
C | CGT | 18 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0175others(15): Show | 18 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.559+13708_559+1370 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13039245 | |||||
| chr19:13039245
|
C | T | 2 | a0001c0001t0003g0085a0001c0001t0003g0161 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559+13693C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039245 | ||||||
| chr19:13039262
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.559+13710A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039262 | ||||||
| chr19:13039494
|
T | C | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01099.hp2 HG01943.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+13942T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039494 | ||||||
| chr19:13039505
|
T | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+13953T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039505 | ||||||
| chr19:13039767
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+14215G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039767 | ||||||
| chr19:13039860
|
G | C | 2 | a0001c0001t0006g0153a0001c0001t0019g0211 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.559+14308G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039860 | ||||||
| chr19:13039977
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+14425C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13039977 | ||||||
| chr19:13040168
|
C | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+14616C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040168 | ||||||
| chr19:13040294
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.559+14742A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040294 | ||||||
| chr19:13040398
|
G | T | 20 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(17): Show | 20 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.559+14846G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040398 | ||||||
| chr19:13040646
|
A | G | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+15094A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040646 | ||||||
| chr19:13040663
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.559+15111T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040663 | ||||||
| chr19:13040784
|
A | G | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.559+15232A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040784 | ||||||
| chr19:13040790
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.559+15238C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040790 | ||||||
| chr19:13040839
|
G | A | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+15287G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040839 | ||||||
| chr19:13040846
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.559+15294A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13040846 | ||||||
| chr19:13041318
|
A | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0151 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.559+15766A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13041318 | ||||||
| chr19:13041793
|
C | CA | 10 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0206others(7): Show | 10 | HG01109.hp2 HG01952.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.559+16258dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13041793 | |||||
| chr19:13041793
|
CAAAAAAA | C | 24 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.559+16252_559+1625 others(11): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13041793 | |||||
| chr19:13042064
|
AT | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.559+16527delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13042064 | |||||
| chr19:13042141
|
C | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.559+16589C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042141 | ||||||
| chr19:13042221
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.559+16669G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042221 | ||||||
| chr19:13042268
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+16716C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042268 | ||||||
| chr19:13042355
|
C | CT | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(208): Show | 211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.559+16823dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13042355 | |||||
| chr19:13042355
|
C | CTT | 23 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(20): Show | 23 | HG00140.hp2 HG00735.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+16822_559+1682 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13042355 | |||||
| chr19:13042417
|
C | T | 1 | a0001c0001t0023g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.559+16865C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042417 | ||||||
| chr19:13042465
|
A | C | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.559+16913A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042465 | ||||||
| chr19:13042511
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.559+16959C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042511 | ||||||
| chr19:13042547
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.559+16995G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042547 | ||||||
| chr19:13042554
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0021g0172 | 2 | HG02970.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.559+17002C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042554 | ||||||
| chr19:13042568
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0055 | 2 | HG00642.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.559+17016G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042568 | ||||||
| chr19:13042569
|
C | G | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.559+17017C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13042569 | ||||||
| chr19:13043785
|
C | T | 20 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(17): Show | 20 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.559+18233C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043785 | ||||||
| chr19:13043804
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0010g0229 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.559+18252G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043804 | ||||||
| chr19:13043870
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+18318A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043870 | ||||||
| chr19:13043890
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.559+18338C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043890 | ||||||
| chr19:13043902
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.559+18350A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043902 | ||||||
| chr19:13043993
|
T | C | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.559+18441T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13043993 | ||||||
| chr19:13044038
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.559+18486G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044038 | ||||||
| chr19:13044047
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.559+18495T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044047 | ||||||
| chr19:13044258
|
G | A | 25 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(22): Show | 25 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.559+18706G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044258 | ||||||
| chr19:13044591
|
A | C | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.559+19039A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044591 | ||||||
| chr19:13044623
|
G | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.559+19071G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044623 | ||||||
| chr19:13044787
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.559+19235C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044787 | ||||||
| chr19:13044886
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+19334A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044886 | ||||||
| chr19:13044895
|
A | G | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.559+19343A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044895 | ||||||
| chr19:13044904
|
C | T | 1 | a0001c0001t0007g0236 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.559+19352C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044904 | ||||||
| chr19:13044953
|
G | A | 1 | a0001c0001t0027g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559+19401G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13044953 | ||||||
| chr19:13045046
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.559+19494C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045046 | ||||||
| chr19:13045047
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+19495G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045047 | ||||||
| chr19:13045130
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.559+19578C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045130 | ||||||
| chr19:13045133
|
G | A | 1 | a0001c0001t0027g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559+19581G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045133 | ||||||
| chr19:13045374
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+19822G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045374 | ||||||
| chr19:13045394
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp1 HG02293.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.559+19842G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045394 | ||||||
| chr19:13045541
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0030g0169 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.559+19989C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045541 | ||||||
| chr19:13045759
|
G | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.559+20207G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045759 | ||||||
| chr19:13045867
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.559+20315G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13045867 | ||||||
| chr19:13046228
|
G | A | 3 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136 | 3 | HG01069.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.559+20676G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046228 | ||||||
| chr19:13046337
|
G | C | 19 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0130others(16): Show | 19 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.559+20785G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046337 | ||||||
| chr19:13046458
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.559+20906G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046458 | ||||||
| chr19:13046466
|
C | G | 76 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.559+20914C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046466 | ||||||
| chr19:13046467
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.559+20915C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046467 | ||||||
| chr19:13046473
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.559+20921C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046473 | ||||||
| chr19:13046473
|
C | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+20921C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046473 | ||||||
| chr19:13046573
|
A | G | 1 | a0001c0001t0004g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.559+21021A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046573 | ||||||
| chr19:13046630
|
T | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01099.hp2 HG01943.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+21078T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046630 | ||||||
| chr19:13046726
|
G | A | 61 | a0001c0001t0001g0024a0001c0001t0001g0065a0001c0001t0001g0067others(58): Show | 61 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.559+21174G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046726 | ||||||
| chr19:13046885
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.559+21333G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13046885 | ||||||
| chr19:13047370
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.559+21818C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047370 | ||||||
| chr19:13047463
|
T | C | 2 | a0001c0001t0013g0227a0001c0001t0013g0231 | 2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.559+21911T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047463 | ||||||
| chr19:13047578
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.559+22026C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047578 | ||||||
| chr19:13047648
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.559+22096C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047648 | ||||||
| chr19:13047754
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0154 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.559+22202A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047754 | ||||||
| chr19:13047829
|
G | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+22277G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047829 | ||||||
| chr19:13047864
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.559+22312T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047864 | ||||||
| chr19:13047866
|
C | T | 1 | a0001c0001t0015g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.559+22314C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047866 | ||||||
| chr19:13047869
|
C | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG01167.hp2 HG01169.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.559+22317C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047869 | ||||||
| chr19:13047919
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0027g0170 | 3 | HG02080.hp1 HG02165.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.559+22367G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047919 | ||||||
| chr19:13047969
|
G | A | 79 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.559+22417G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13047969 | ||||||
| chr19:13048382
|
C | T | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.559+22830C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048382 | ||||||
| chr19:13048472
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.559+22920C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048472 | ||||||
| chr19:13048483
|
AT | A | 22 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(19): Show | 22 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+22943delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13048483 | |||||
| chr19:13048638
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.559+23086T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048638 | ||||||
| chr19:13048731
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0008g0006others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+23179G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048731 | ||||||
| chr19:13048755
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.559+23203A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048755 | ||||||
| chr19:13048904
|
C | T | 1 | a0001c0001t0021g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559+23352C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048904 | ||||||
| chr19:13048968
|
T | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp1 HG02293.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.559+23416T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13048968 | ||||||
| chr19:13049045
|
C | G | 12 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0107others(9): Show | 12 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.559+23493C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049045 | ||||||
| chr19:13049080
|
A | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.559+23528A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049080 | ||||||
| chr19:13049084
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.559+23532A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049084 | ||||||
| chr19:13049158
|
C | T | 1 | a0001c0001t0016g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.559+23606C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049158 | ||||||
| chr19:13049176
|
C | G | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.559+23624C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049176 | ||||||
| chr19:13049236
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.559+23684A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049236 | ||||||
| chr19:13049470
|
T | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-23577T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049470 | ||||||
| chr19:13049482
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.560-23565G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049482 | ||||||
| chr19:13049527
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0146a0001c0001t0001g0165 | 3 | HG00408.hp1 HG00438.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.560-23520G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049527 | ||||||
| chr19:13049595
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.560-23436delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13049595 | |||||
| chr19:13049595
|
CTT | C | 5 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0107others(2): Show | 5 | HG01255.hp2 HG02572.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.560-23437_560-2343 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13049595 | |||||
| chr19:13049709
|
T | C | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-23338T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049709 | ||||||
| chr19:13049711
|
G | C | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-23336G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049711 | ||||||
| chr19:13049742
|
C | T | 8 | a0001c0001t0004g0017a0001c0001t0004g0091a0001c0001t0004g0092others(5): Show | 8 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.560-23305C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049742 | ||||||
| chr19:13049849
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-23198C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13049849 | ||||||
| chr19:13050058
|
C | T | 1 | a0001c0001t0029g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.560-22989C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050058 | ||||||
| chr19:13050407
|
C | T | 3 | a0001c0001t0007g0236a0001c0001t0007g0237a0001c0001t0007g0238 | 3 | NA19012.hp2 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.560-22640C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050407 | ||||||
| chr19:13050449
|
C | T | 2 | a0001c0001t0006g0153a0001c0001t0019g0211 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560-22598C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050449 | ||||||
| chr19:13050592
|
T | A | 1 | a0001c0001t0002g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560-22455T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050592 | ||||||
| chr19:13050657
|
A | G | 1 | a0001c0001t0005g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.560-22390A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050657 | ||||||
| chr19:13050855
|
G | A | 10 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 10 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.560-22192G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050855 | ||||||
| chr19:13050960
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.560-22087A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13050960 | ||||||
| chr19:13051154
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.560-21893G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051154 | ||||||
| chr19:13051334
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.560-21713G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051334 | ||||||
| chr19:13051541
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0036g0011 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.560-21506G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051541 | ||||||
| chr19:13051759
|
A | G | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560-21288A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051759 | ||||||
| chr19:13051823
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.560-21224C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051823 | ||||||
| chr19:13051858
|
GGGGCGGC others(14): Show |
G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.560-21180_560-2116 others(25): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13051858 | |||||
| chr19:13051862
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.560-21185C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13051862 | ||||||
| chr19:13052077
|
C | A | 1 | a0001c0001t0003g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560-20970C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052077 | ||||||
| chr19:13052212
|
C | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-20835C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052212 | ||||||
| chr19:13052346
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-20701C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052346 | ||||||
| chr19:13052353
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0027others(1): Show | 4 | HG02572.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-20694G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052353 | ||||||
| chr19:13052701
|
T | C | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.560-20346T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052701 | ||||||
| chr19:13052730
|
T | C | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-20317T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052730 | ||||||
| chr19:13052743
|
ACGGCT | A | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.560-20297_560-2029 others(9): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13052743 | |||||
| chr19:13052762
|
G | A | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.560-20285G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052762 | ||||||
| chr19:13052923
|
G | A | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-20124G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052923 | ||||||
| chr19:13052957
|
A | G | 1 | a0001c0001t0022g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.560-20090A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13052957 | ||||||
| chr19:13053149
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.560-19898G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053149 | ||||||
| chr19:13053214
|
G | A | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-19833G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053214 | ||||||
| chr19:13053349
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-19698A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053349 | ||||||
| chr19:13053373
|
T | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-19674T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053373 | ||||||
| chr19:13053512
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-19535G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053512 | ||||||
| chr19:13053760
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.560-19287A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053760 | ||||||
| chr19:13053781
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.560-19266C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053781 | ||||||
| chr19:13053947
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.560-19100C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13053947 | ||||||
| chr19:13054141
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.560-18906G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054141 | ||||||
| chr19:13054149
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0242 | 3 | HG02055.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560-18898C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054149 | ||||||
| chr19:13054349
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.560-18698A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054349 | ||||||
| chr19:13054379
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-18668C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054379 | ||||||
| chr19:13054408
|
G | C | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-18639G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054408 | ||||||
| chr19:13054496
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.560-18551G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054496 | ||||||
| chr19:13054583
|
G | A | 6 | a0001c0001t0001g0213a0001c0001t0012g0212a0001c0001t0012g0214others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-18464G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054583 | ||||||
| chr19:13054707
|
T | C | 1 | a0001c0001t0001g0241 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.560-18340T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054707 | ||||||
| chr19:13054718
|
G | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-18329G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054718 | ||||||
| chr19:13054742
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.560-18305G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054742 | ||||||
| chr19:13054755
|
A | C | 18 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.560-18292A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054755 | ||||||
| chr19:13054827
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.560-18220C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13054827 | ||||||
| chr19:13055070
|
C | T | 41 | a0001c0001t0001g0024a0001c0001t0001g0065a0001c0001t0001g0067others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.560-17977C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055070 | ||||||
| chr19:13055178
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-17869T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055178 | ||||||
| chr19:13055193
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-17854G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055193 | ||||||
| chr19:13055194
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-17853C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055194 | ||||||
| chr19:13055198
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-17849A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055198 | ||||||
| chr19:13055226
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.560-17821C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055226 | ||||||
| chr19:13055339
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.560-17708T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055339 | ||||||
| chr19:13055344
|
C | T | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.560-17703C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055344 | ||||||
| chr19:13055666
|
G | A | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0062others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-17381G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055666 | ||||||
| chr19:13055740
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.560-17307C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055740 | ||||||
| chr19:13055874
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.560-17173C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13055874 | ||||||
| chr19:13056066
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0233 | 2 | NA18990.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.560-16981G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056066 | ||||||
| chr19:13056150
|
A | G | 1 | a0001c0001t0027g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560-16897A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056150 | ||||||
| chr19:13056247
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-16800G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056247 | ||||||
| chr19:13056261
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-16786G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056261 | ||||||
| chr19:13056262
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-16785A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056262 | ||||||
| chr19:13056263
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-16784G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056263 | ||||||
| chr19:13056544
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.560-16503C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056544 | ||||||
| chr19:13056574
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.560-16473G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056574 | ||||||
| chr19:13056745
|
C | T | 7 | a0001c0001t0004g0017a0001c0001t0004g0091a0001c0001t0004g0092others(4): Show | 7 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.560-16302C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056745 | ||||||
| chr19:13056886
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.560-16161G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13056886 | ||||||
| chr19:13057076
|
C | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.560-15971C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057076 | ||||||
| chr19:13057256
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560-15791C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057256 | ||||||
| chr19:13057276
|
G | A | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-15771G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057276 | ||||||
| chr19:13057477
|
TCGGCTTT others(8): Show |
T | 1 | a0001c0001t0005g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560-15568_560-1555 others(19): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13057477 | |||||
| chr19:13057527
|
G | T | 2 | a0001c0001t0006g0153a0001c0001t0019g0211 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560-15520G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057527 | ||||||
| chr19:13057543
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560-15504G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057543 | ||||||
| chr19:13057809
|
C | CCT | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.560-15237_560-1523 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13057809 | |||||
| chr19:13057824
|
C | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-15223C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057824 | ||||||
| chr19:13057834
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.560-15213G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13057834 | ||||||
| chr19:13058325
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560-14722G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13058325 | ||||||
| chr19:13058365
|
C | T | 3 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243 | 3 | HG02559.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.560-14682C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13058365 | ||||||
| chr19:13058751
|
G | A | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560-14296G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13058751 | ||||||
| chr19:13058826
|
G | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560-14221G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13058826 | ||||||
| chr19:13058840
|
GGTAGGTC others(3): Show |
G | 1 | a0001c0001t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.560-14205_560-1419 others(14): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13058840 | |||||
| chr19:13059074
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-13973G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059074 | ||||||
| chr19:13059113
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | NA18966.hp2 NA18990.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.560-13934T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059113 | ||||||
| chr19:13059235
|
A | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560-13812A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059235 | ||||||
| chr19:13059283
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.560-13764G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059283 | ||||||
| chr19:13059305
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-13742G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059305 | ||||||
| chr19:13059410
|
C | T | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.560-13637C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059410 | ||||||
| chr19:13059648
|
A | G | 4 | a0001c0001t0001g0247a0001c0001t0011g0251a0001c0001t0011g0252others(1): Show | 4 | HG01192.hp2 HG01243.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-13399A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13059648 | ||||||
| chr19:13059739
|
C | CT | 7 | a0001c0001t0001g0063a0001c0001t0001g0107a0001c0001t0001g0221others(4): Show | 7 | HG00735.hp1 HG01255.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.560-13293dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059739 | |||||
| chr19:13059739
|
CT | C | 24 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG01192.hp2 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.560-13293delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059739 | |||||
| chr19:13059777
|
C | CT | 35 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0027others(32): Show | 35 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.560-13246dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059777 | |||||
| chr19:13059777
|
C | CTT | 5 | a0001c0001t0001g0096a0001c0001t0001g0104a0001c0001t0001g0108others(2): Show | 5 | HG00323.hp1 NA18962.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.560-13247_560-1324 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059777 | |||||
| chr19:13059777
|
CT | C | 80 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.560-13246delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059777 | |||||
| chr19:13059777
|
CTT | C | 12 | a0001c0001t0001g0071a0001c0001t0001g0175a0001c0001t0001g0176others(9): Show | 12 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.560-13247_560-1324 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059777 | |||||
| chr19:13059777
|
CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0001g0115a0001c0001t0001g0149a0001c0001t0001g0151others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.560-13257_560-1324 others(16): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13059777 | |||||
| chr19:13060298
|
T | C | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.560-12749T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13060298 | ||||||
| chr19:13060341
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.560-12706G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13060341 | ||||||
| chr19:13060610
|
T | C | 23 | a0001c0001t0001g0076a0001c0001t0002g0128a0001c0001t0002g0135others(20): Show | 23 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.560-12437T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13060610 | ||||||
| chr19:13060771
|
C | A | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.560-12276C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13060771 | ||||||
| chr19:13060778
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.560-12269A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13060778 | ||||||
| chr19:13061020
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.560-12027C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13061020 | ||||||
| chr19:13061082
|
AC | A | 103 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(100): Show | 103 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.560-11957delC | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13061082 | |||||
| chr19:13061084
|
C | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.560-11963C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13061084 | ||||||
| chr19:13061092
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.560-11955C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13061092 | ||||||
| chr19:13061639
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-11408C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13061639 | ||||||
| chr19:13061912
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.560-11135G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13061912 | ||||||
| chr19:13062497
|
G | A | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-10550G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13062497 | ||||||
| chr19:13062757
|
A | C | 1 | a0001c0001t0005g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.560-10290A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13062757 | ||||||
| chr19:13063036
|
T | C | 10 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.560-10011T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063036 | ||||||
| chr19:13063102
|
G | C | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-9945G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063102 | ||||||
| chr19:13063132
|
G | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-9915G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063132 | ||||||
| chr19:13063301
|
C | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-9746C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063301 | ||||||
| chr19:13063482
|
GT | G | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.560-9554delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13063482 | |||||
| chr19:13063498
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.560-9549G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063498 | ||||||
| chr19:13063545
|
T | C | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-9502T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063545 | ||||||
| chr19:13063862
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-9185G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13063862 | ||||||
| chr19:13064073
|
GA | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.560-8973delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064073 | ||||||
| chr19:13064074
|
AC | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.560-8964delC | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13064074 | |||||
| chr19:13064083
|
C | A | 1 | a0001c0001t0002g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560-8964C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064083 | ||||||
| chr19:13064193
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0210a0001c0001t0001g0215 | 3 | HG00639.hp1 HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.560-8854C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064193 | ||||||
| chr19:13064316
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-8731C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064316 | ||||||
| chr19:13064370
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-8677G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064370 | ||||||
| chr19:13064535
|
T | C | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-8512T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064535 | ||||||
| chr19:13064801
|
A | C | 16 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(13): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.560-8246A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064801 | ||||||
| chr19:13064847
|
G | A | 1 | a0001c0001t0023g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560-8200G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13064847 | ||||||
| chr19:13065037
|
G | C | 1 | a0001c0001t0001g0241 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.560-8010G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065037 | ||||||
| chr19:13065046
|
T | TC | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.560-8001_560-8000i others(3): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065046 | ||||||
| chr19:13065206
|
G | T | 13 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(10): Show | 13 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.560-7841G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065206 | ||||||
| chr19:13065295
|
G | A | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560-7752G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065295 | ||||||
| chr19:13065365
|
G | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-7682G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065365 | ||||||
| chr19:13065441
|
C | T | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-7606C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065441 | ||||||
| chr19:13065480
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560-7567G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065480 | ||||||
| chr19:13065596
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.560-7451T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065596 | ||||||
| chr19:13065914
|
C | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.560-7133C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13065914 | ||||||
| chr19:13066001
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.560-7046T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066001 | ||||||
| chr19:13066330
|
G | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0192 | 3 | HG02129.hp2 HG02132.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.560-6717G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066330 | ||||||
| chr19:13066353
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.560-6694C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066353 | ||||||
| chr19:13066373
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.560-6674G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066373 | ||||||
| chr19:13066390
|
G | A | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-6657G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066390 | ||||||
| chr19:13066446
|
C | T | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.560-6601C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066446 | ||||||
| chr19:13066652
|
G | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.560-6395G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13066652 | ||||||
| chr19:13067070
|
C | G | 2 | a0001c0001t0014g0171a0001c0001t0014g0217 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560-5977C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067070 | ||||||
| chr19:13067076
|
C | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-5971C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067076 | ||||||
| chr19:13067465
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0008g0209 | 2 | HG01993.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.560-5582T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067465 | ||||||
| chr19:13067481
|
TGC | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-5564_560-5563d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13067481 | |||||
| chr19:13067483
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0002g0235 | 3 | HG02602.hp1 HG02895.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.560-5564C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067483 | ||||||
| chr19:13067483
|
CGT | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.560-5543_560-5542d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13067483 | |||||
| chr19:13067483
|
CGTGT | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0084a0001c0001t0001g0194others(22): Show | 25 | HG01169.hp2 HG01516.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.560-5545_560-5542d others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13067483 | |||||
| chr19:13067485
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0147others(1): Show | 4 | HG01109.hp1 HG02602.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-5562T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067485 | ||||||
| chr19:13067487
|
T | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-5560T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067487 | ||||||
| chr19:13067489
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG00438.hp1 HG02165.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-5558T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067489 | ||||||
| chr19:13067758
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560-5289A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067758 | ||||||
| chr19:13067796
|
A | AAT | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0027others(2): Show | 5 | HG02572.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.560-5236_560-5235d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 13067796 | |||||
| chr19:13067830
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.560-5217G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067830 | ||||||
| chr19:13067955
|
A | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0210a0001c0001t0001g0215 | 3 | HG00639.hp1 HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.560-5092A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13067955 | ||||||
| chr19:13068017
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560-5030A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068017 | ||||||
| chr19:13068043
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.560-5004T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068043 | ||||||
| chr19:13068053
|
C | G | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-4994C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068053 | ||||||
| chr19:13068059
|
C | T | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-4988C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068059 | ||||||
| chr19:13068114
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.560-4933A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068114 | ||||||
| chr19:13068652
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.560-4395A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068652 | ||||||
| chr19:13068669
|
A | G | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.560-4378A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068669 | ||||||
| chr19:13068796
|
C | T | 11 | a0001c0001t0001g0115a0001c0001t0001g0149a0001c0001t0001g0151others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.560-4251C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068796 | ||||||
| chr19:13068838
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.560-4209A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068838 | ||||||
| chr19:13068846
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.560-4201C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068846 | ||||||
| chr19:13068848
|
C | A | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.560-4199C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068848 | ||||||
| chr19:13068876
|
G | A | 1 | a0001c0001t0023g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560-4171G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13068876 | ||||||
| chr19:13069027
|
G | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0008g0201 | 3 | NA18962.hp1 NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.560-4020G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069027 | ||||||
| chr19:13069055
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-3992A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069055 | ||||||
| chr19:13069085
|
T | G | 1 | a0001c0001t0031g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.560-3962T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069085 | ||||||
| chr19:13069144
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.560-3903C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069144 | ||||||
| chr19:13069245
|
G | A | 1 | a0001c0001t0005g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560-3802G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069245 | ||||||
| chr19:13069588
|
G | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0022g0088 | 3 | HG02056.hp1 NA19003.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.560-3459G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069588 | ||||||
| chr19:13069647
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.560-3400C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13069647 | ||||||
| chr19:13070049
|
G | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.560-2998G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070049 | ||||||
| chr19:13070110
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.560-2937C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070110 | ||||||
| chr19:13070267
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.560-2780T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070267 | ||||||
| chr19:13070315
|
G | A | 1 | a0001c0001t0027g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560-2732G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070315 | ||||||
| chr19:13070410
|
C | T | 3 | a0001c0001t0003g0150a0001c0001t0003g0181a0001c0001t0003g0216 | 3 | HG02486.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.560-2637C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070410 | ||||||
| chr19:13070494
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.560-2553C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070494 | ||||||
| chr19:13070974
|
A | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0146a0001c0001t0001g0165 | 3 | HG00408.hp1 HG00438.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.560-2073A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070974 | ||||||
| chr19:13070976
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.560-2071C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13070976 | ||||||
| chr19:13071282
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.560-1765C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13071282 | ||||||
| chr19:13071292
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.560-1755C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13071292 | ||||||
| chr19:13071463
|
G | A | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560-1584G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13071463 | ||||||
| chr19:13071818
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.560-1229C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13071818 | ||||||
| chr19:13071855
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560-1192A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13071855 | ||||||
| chr19:13072052
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.560-995C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072052 | ||||||
| chr19:13072186
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.560-861C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072186 | ||||||
| chr19:13072895
|
T | A | 2 | a0001c0001t0001g0012a0001c0001t0036g0011 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.560-152T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072895 | ||||||
| chr19:13072915
|
G | C | 2 | a0001c0001t0014g0171a0001c0001t0014g0217 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.560-132G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072915 | ||||||
| chr19:13072948
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.560-99C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072948 | ||||||
| chr19:13072956
|
C | T | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.560-91C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 2/10 | chr19 | 13072956 | ||||||
| chr19:13073135
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.622+26G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 3/10 | chr19 | 13073135 | ||||||
| chr19:13073285
|
G | A | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.623-137G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 3/10 | chr19 | 13073285 | ||||||
| chr19:13073387
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0045 | 2 | HG00408.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.623-35C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 3/10 | chr19 | 13073387 | ||||||
| chr19:13073545
|
A | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.697+49A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 4/10 | chr19 | 13073545 | ||||||
| chr19:13073589
|
G | A | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.697+93G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 4/10 | chr19 | 13073589 | ||||||
| chr19:13073738
|
A | G | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-168A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 4/10 | chr19 | 13073738 | ||||||
| chr19:13074104
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0064 | 2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.818+78C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074104 | ||||||
| chr19:13074155
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.818+129C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074155 | ||||||
| chr19:13074195
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.818+169C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074195 | ||||||
| chr19:13074305
|
A | T | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.818+279A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074305 | ||||||
| chr19:13074672
|
A | G | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.818+646A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074672 | ||||||
| chr19:13074675
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.818+649G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074675 | ||||||
| chr19:13074719
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.818+693T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074719 | ||||||
| chr19:13074720
|
A | T | 1 | a0001c0001t0005g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.818+694A>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074720 | ||||||
| chr19:13074819
|
C | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.819-716C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074819 | ||||||
| chr19:13074901
|
C | T | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.819-634C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074901 | ||||||
| chr19:13074914
|
C | T | 2 | a0001c0001t0006g0153a0001c0001t0019g0211 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.819-621C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074914 | ||||||
| chr19:13074930
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.819-605C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13074930 | ||||||
| chr19:13075026
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0154a0001c0001t0019g0211 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.819-509C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13075026 | ||||||
| chr19:13075068
|
T | TA | 23 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0099others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-446dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr19 | 13075068 | |||||
| chr19:13075068
|
T | TAAAAAA | 12 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.819-451_819-446dup others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr19 | 13075068 | |||||
| chr19:13075068
|
T | TAAAAAAA | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(40): Show | 43 | HG00323.hp2 HG01069.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.819-452_819-446dup others(7): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr19 | 13075068 | |||||
| chr19:13075068
|
T | TAAAAAAA others(1): Show |
57 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.819-453_819-446dup others(8): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr19 | 13075068 | |||||
| chr19:13075068
|
T | TAAAAAAA others(2): Show |
14 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00408.hp2 HG00673.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.819-454_819-446dup others(9): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr19 | 13075068 | |||||
| chr19:13075386
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0044 | 2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.819-149C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13075386 | ||||||
| chr19:13075455
|
G | A | 1 | a0001c0001t0016g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.819-80G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13075455 | ||||||
| chr19:13075497
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.819-38C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 5/10 | chr19 | 13075497 | ||||||
| chr19:13075709
|
G | A | 1 | a0001c0001t0006g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.955+38G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13075709 | ||||||
| chr19:13075710
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.955+39C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13075710 | ||||||
| chr19:13075813
|
C | T | 1 | a0001c0001t0019g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.955+142C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13075813 | ||||||
| chr19:13075860
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.955+189A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13075860 | ||||||
| chr19:13075945
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.955+274G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13075945 | ||||||
| chr19:13076009
|
T | G | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.955+338T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076009 | ||||||
| chr19:13076034
|
C | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0245 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955+363C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076034 | ||||||
| chr19:13076153
|
G | A | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.955+482G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076153 | ||||||
| chr19:13076318
|
A | G | 16 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(13): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.955+647A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076318 | ||||||
| chr19:13076392
|
C | T | 1 | a0001c0001t0014g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.955+721C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076392 | ||||||
| chr19:13076455
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.955+784C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076455 | ||||||
| chr19:13076768
|
G | T | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.955+1097G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076768 | ||||||
| chr19:13076859
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.955+1188C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076859 | ||||||
| chr19:13076895
|
C | A | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.955+1224C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076895 | ||||||
| chr19:13076896
|
C | G | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.955+1225C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076896 | ||||||
| chr19:13076974
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.955+1303G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13076974 | ||||||
| chr19:13077145
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.956-1468A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077145 | ||||||
| chr19:13077241
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.956-1372C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077241 | ||||||
| chr19:13077476
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.956-1137A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077476 | ||||||
| chr19:13077696
|
C | A | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956-917C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077696 | ||||||
| chr19:13077702
|
C | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.956-911C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077702 | ||||||
| chr19:13077853
|
C | G | 1 | a0001c0001t0019g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.956-760C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13077853 | ||||||
| chr19:13078534
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.956-79G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13078534 | ||||||
| chr19:13078549
|
C | T | 10 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.956-64C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 6/10 | chr19 | 13078549 | ||||||
| chr19:13078780
|
T | TGAGTATC others(15): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078+46_1078+67dup others(22): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 13078780 | |||||
| chr19:13078824
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1078+89C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13078824 | ||||||
| chr19:13078902
|
C | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+167C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13078902 | ||||||
| chr19:13078938
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1078+203G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13078938 | ||||||
| chr19:13079115
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1078+380T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13079115 | ||||||
| chr19:13079788
|
A | G | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1078+1053A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13079788 | ||||||
| chr19:13079906
|
G | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078+1171G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13079906 | ||||||
| chr19:13079926
|
A | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1078+1191A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13079926 | ||||||
| chr19:13079974
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1078+1239A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13079974 | ||||||
| chr19:13080000
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1078+1265G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080000 | ||||||
| chr19:13080216
|
CA | C | 29 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 29 | HG01192.hp2 HG01243.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1079-1456delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 13080216 | |||||
| chr19:13080358
|
C | T | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1079-1322C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080358 | ||||||
| chr19:13080647
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1079-1033C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080647 | ||||||
| chr19:13080660
|
T | C | 3 | a0001c0001t0001g0247a0001c0001t0020g0244a0001c0001t0024g0119 | 3 | HG03471.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1079-1020T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080660 | ||||||
| chr19:13080690
|
C | T | 3 | a0001c0001t0002g0159a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG03710.hp1 HG04115.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1079-990C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080690 | ||||||
| chr19:13080729
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1079-951G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080729 | ||||||
| chr19:13080748
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1079-932C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080748 | ||||||
| chr19:13080799
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1079-881G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080799 | ||||||
| chr19:13080832
|
C | T | 22 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(19): Show | 22 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1079-848C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080832 | ||||||
| chr19:13080856
|
C | T | 16 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(13): Show | 16 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1079-824C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13080856 | ||||||
| chr19:13081461
|
G | GATT | 4 | a0001c0001t0001g0078a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00741.hp1 HG02293.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1079-200_1079-198d others(5): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 13081461 | |||||
| chr19:13081483
|
T | A | 7 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-197T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13081483 | ||||||
| chr19:13081582
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0020g0244 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1079-98C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13081582 | ||||||
| chr19:13081600
|
A | G | 22 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(19): Show | 22 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1079-80A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13081600 | ||||||
| chr19:13081650
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1079-30G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 7/10 | chr19 | 13081650 | ||||||
| chr19:13081927
|
C | A | 4 | a0001c0001t0003g0174a0001c0001t0003g0177a0001c0001t0003g0179others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+72C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13081927 | ||||||
| chr19:13081994
|
C | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+139C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13081994 | ||||||
| chr19:13082189
|
G | T | 9 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 9 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+334G>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082189 | ||||||
| chr19:13082285
|
T | C | 2 | a0001c0001t0006g0168a0001c0001t0006g0182 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1254+430T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082285 | ||||||
| chr19:13082372
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1254+517C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082372 | ||||||
| chr19:13082939
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1254+1084A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082939 | ||||||
| chr19:13082968
|
G | A | 20 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(17): Show | 20 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1254+1113G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082968 | ||||||
| chr19:13082970
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0002t0001g0019others(1): Show | 4 | HG03654.hp2 HG03834.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+1115C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13082970 | ||||||
| chr19:13083032
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1254+1177C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083032 | ||||||
| chr19:13083247
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1254+1392G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083247 | ||||||
| chr19:13083636
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1254+1781A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083636 | ||||||
| chr19:13083649
|
G | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0203a0001c0001t0001g0205 | 3 | HG01169.hp2 HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1254+1794G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083649 | ||||||
| chr19:13083704
|
TTGTGTGG others(2): Show |
T | 4 | a0001c0001t0001g0070a0001c0001t0011g0251a0001c0001t0011g0252others(1): Show | 4 | HG01192.hp2 HG01243.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+1862_1254+187 others(13): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13083704 | |||||
| chr19:13083870
|
C | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG01934.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+2015C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083870 | ||||||
| chr19:13083877
|
C | G | 2 | a0001c0001t0002g0230a0001c0001t0010g0229 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1254+2022C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083877 | ||||||
| chr19:13083956
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1254+2101C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083956 | ||||||
| chr19:13083958
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1254+2103C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083958 | ||||||
| chr19:13083967
|
A | G | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1254+2112A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13083967 | ||||||
| chr19:13084467
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1254+2612A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13084467 | ||||||
| chr19:13084469
|
A | C | 3 | a0001c0001t0001g0247a0001c0001t0017g0160a0001c0001t0020g0244 | 3 | HG03688.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1254+2614A>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13084469 | ||||||
| chr19:13084735
|
T | A | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1254+2880T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13084735 | ||||||
| chr19:13084796
|
G | A | 1 | a0001c0001t0031g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1254+2941G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13084796 | ||||||
| chr19:13085027
|
G | A | 1 | a0001c0001t0029g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1255-2962G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085027 | ||||||
| chr19:13085069
|
C | CA | 22 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0039others(19): Show | 22 | HG00738.hp1 HG01934.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1255-2898dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13085069 | |||||
| chr19:13085105
|
C | T | 1 | a0001c0001t0014g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1255-2884C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085105 | ||||||
| chr19:13085322
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0191others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-2667C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085322 | ||||||
| chr19:13085470
|
C | T | 1 | a0001c0001t0006g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1255-2519C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085470 | ||||||
| chr19:13085472
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1255-2517T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085472 | ||||||
| chr19:13085613
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1255-2376T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085613 | ||||||
| chr19:13085654
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255-2335T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085654 | ||||||
| chr19:13085831
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0006g0153 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1255-2158C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085831 | ||||||
| chr19:13085832
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-2157G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13085832 | ||||||
| chr19:13086135
|
C | T | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-1854C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086135 | ||||||
| chr19:13086275
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1255-1714C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086275 | ||||||
| chr19:13086341
|
C | T | 3 | a0001c0001t0001g0026a0001c0002t0001g0019a0001c0002t0001g0080 | 3 | HG03654.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1255-1648C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086341 | ||||||
| chr19:13086445
|
T | A | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1255-1544T>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086445 | ||||||
| chr19:13086650
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1255-1339C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086650 | ||||||
| chr19:13086674
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1255-1315G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086674 | ||||||
| chr19:13086865
|
G | A | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-1124G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086865 | ||||||
| chr19:13086938
|
C | T | 20 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0176others(17): Show | 20 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-1051C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086938 | ||||||
| chr19:13086977
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0145a0001c0001t0015g0132 | 3 | HG03239.hp1 HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1255-1012G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13086977 | ||||||
| chr19:13087457
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1255-532C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13087457 | ||||||
| chr19:13087515
|
C | T | 2 | a0001c0001t0019g0211a0001c0001t0020g0244 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1255-474C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13087515 | ||||||
| chr19:13087774
|
C | CA | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1255-191dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13087774 | |||||
| chr19:13087774
|
C | CAA | 18 | a0001c0001t0001g0014a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG01358.hp2 HG01433.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1255-192_1255-191d others(4): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13087774 | |||||
| chr19:13087774
|
C | CAAA | 11 | a0001c0001t0001g0084a0001c0001t0001g0247a0001c0001t0003g0081others(8): Show | 11 | HG01934.hp1 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-193_1255-191d others(5): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13087774 | |||||
| chr19:13087774
|
CA | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0087a0001c0001t0001g0108others(5): Show | 8 | HG01069.hp2 HG01981.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-191delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13087774 | |||||
| chr19:13087774
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1255-201_1255-191d others(13): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr19 | 13087774 | |||||
| chr19:13087887
|
G | A | 18 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0178others(15): Show | 18 | HG01934.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1255-102G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 8/10 | chr19 | 13087887 | ||||||
| chr19:13088146
|
C | T | 1 | a0001c0001t0034g0020 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1402+10C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088146 | ||||||
| chr19:13088352
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1402+216T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088352 | ||||||
| chr19:13088489
|
G | GT | 5 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(2): Show | 5 | HG01934.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+366dupT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 13088489 | |||||
| chr19:13088489
|
GT | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0104a0001c0001t0001g0108others(3): Show | 6 | HG01358.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+366delT | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 13088489 | |||||
| chr19:13088496
|
T | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0079others(14): Show | 17 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1402+360T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088496 | ||||||
| chr19:13088538
|
T | C | 1 | a0001c0001t0004g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1402+402T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088538 | ||||||
| chr19:13088664
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1402+528C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088664 | ||||||
| chr19:13088719
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1402+583T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088719 | ||||||
| chr19:13088742
|
G | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1402+606G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13088742 | ||||||
| chr19:13089092
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1402+956G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13089092 | ||||||
| chr19:13089195
|
G | C | 1 | a0001c0001t0020g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402+1059G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13089195 | ||||||
| chr19:13089297
|
C | T | 1 | a0001c0001t0008g0209 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1403-1002C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13089297 | ||||||
| chr19:13089907
|
G | A | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1403-392G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13089907 | ||||||
| chr19:13090163
|
C | G | 6 | a0001c0001t0006g0168a0001c0001t0006g0182a0001c0001t0006g0243others(3): Show | 6 | HG01934.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1403-136C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 9/10 | chr19 | 13090163 | ||||||
| chr19:13090668
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1494+278G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13090668 | ||||||
| chr19:13090670
|
C | T | 4 | a0001c0001t0002g0235a0001c0001t0007g0236a0001c0001t0007g0237others(1): Show | 4 | HG02602.hp1 NA19012.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+280C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13090670 | ||||||
| chr19:13090750
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0003g0081a0001c0001t0003g0082others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+360C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13090750 | ||||||
| chr19:13090792
|
G | A | 21 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(18): Show | 21 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1494+402G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13090792 | ||||||
| chr19:13090810
|
C | T | 7 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1494+420C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13090810 | ||||||
| chr19:13091023
|
C | T | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1494+633C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13091023 | ||||||
| chr19:13091053
|
G | A | 1 | a0001c0001t0023g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1494+663G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13091053 | ||||||
| chr19:13091374
|
T | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1494+984T>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13091374 | ||||||
| chr19:13091400
|
C | CA | 23 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0061others(20): Show | 23 | HG00673.hp1 HG00735.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1494+1030dupA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr19 | 13091400 | |||||
| chr19:13091400
|
C | CAA | 8 | a0001c0001t0003g0085a0001c0001t0006g0168a0001c0001t0006g0182others(5): Show | 8 | HG01934.hp2 HG02559.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1494+1029_1494+103 others(6): Show |
NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr19 | 13091400 | |||||
| chr19:13091400
|
CA | C | 5 | a0001c0001t0001g0028a0001c0001t0003g0181a0001c0001t0003g0216others(2): Show | 5 | HG00140.hp2 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+1030delA | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr19 | 13091400 | |||||
| chr19:13092072
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1494+1682G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092072 | ||||||
| chr19:13092525
|
C | A | 1 | a0001c0001t0017g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1495-2110C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092525 | ||||||
| chr19:13092531
|
C | A | 6 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG01934.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-2104C>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092531 | ||||||
| chr19:13092653
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1495-1982G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092653 | ||||||
| chr19:13092677
|
A | G | 2 | a0001c0001t0003g0174a0001c0001t0003g0179 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1495-1958A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092677 | ||||||
| chr19:13092810
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1495-1825C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092810 | ||||||
| chr19:13092846
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1495-1789C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092846 | ||||||
| chr19:13092858
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1495-1777G>A | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13092858 | ||||||
| chr19:13093420
|
G | C | 6 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG01934.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-1215G>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13093420 | ||||||
| chr19:13093565
|
C | T | 1 | a0001c0001t0030g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1495-1070C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13093565 | ||||||
| chr19:13093590
|
T | C | 3 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0030g0169 | 3 | HG01192.hp2 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1495-1045T>C | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13093590 | ||||||
| chr19:13093600
|
C | G | 2 | a0001c0001t0011g0251a0001c0001t0011g0252 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1495-1035C>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13093600 | ||||||
| chr19:13094021
|
A | G | 5 | a0001c0001t0011g0251a0001c0001t0011g0252a0001c0001t0019g0211others(2): Show | 5 | HG01192.hp2 HG01243.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-614A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13094021 | ||||||
| chr19:13094201
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1495-434A>G | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13094201 | ||||||
| chr19:13094239
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1495-396C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 10/10 | chr19 | 13094239 |