Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1506 | 250 | 80 | 64 | 62 | 6 | 36 | NFIX_chr19_12990475_13103796 | NFIX | ATGTA others(1501): Show |
chr19 | 12990475 | 13103796 | ||
| a0001c0002 | 0/0 | 1506 | 2 | 0 | 0 | 0 | 0 | 2 | NFIX_chr19_12990475_13103796 | NFIX | ATGTA others(1501): Show |
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 | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0002 | 0/0 | 6020 | 14 | 1 | 5 | 3 | 0 | 5 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6015): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0003 | 0/0 | 6018 | 14 | 13 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0004 | 0/0 | 6019 | 8 | 0 | 5 | 0 | 2 | 1 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0005 | 0/0 | 6019 | 6 | 5 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0006 | 0/0 | 6019 | 4 | 4 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0007 | 0/0 | 6020 | 3 | 0 | 0 | 3 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6015): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0008 | 0/0 | 6020 | 3 | 1 | 0 | 2 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6015): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0009 | 0/0 | 6019 | 3 | 3 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0010 | 0/0 | 6021 | 2 | 0 | 0 | 1 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6016): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0011 | 0/0 | 6018 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0012 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6010): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0013 | 0/0 | 6020 | 2 | 0 | 2 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6015): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0014 | 0/0 | 6019 | 2 | 2 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0015 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0016 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0017 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0018 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0019 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0020 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0021 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0022 | 0/0 | 6019 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0023 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0024 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0025 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0026 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0027 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0028 | 0/0 | 6019 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0029 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0030 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0031 | 0/0 | 6018 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0032 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0033 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6010): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0034 | 0/0 | 6019 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0035 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6013): Show |
chr19 | 12990475 | 13103796 |
| a0001c0001t0036 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
chr19 | 12990475 | 13103796 |
| a0001c0002t0001 | 0/0 | 6019 | 2 | 0 | 0 | 0 | 0 | 2 | NFIX_chr19_12990475_13103796 | NFIX | GTCTA others(6014): Show |
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 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0105 | 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 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| a0001c0001t0001g0133 | 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 |
| a0001c0001t0004g0106 | 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 |
| a0001c0001t0015g0134 | 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 | g0106 | 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 | g0103 | 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 | g0099 | 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 | g0133 | 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 | g0102 | 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 | g0098 | 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 | g0104 | 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 | g0100 | 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 | g0134 | 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 | g0132 | 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 | g0105 | 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 | a0001 | c0001 | t0001 | g0241 | REF | REF | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0204 | REF | REF | NFIX_chr19_12990475_13103796 | NFIX | chr19 | 12990475 | 13103796 |
| view | 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 |
|---|
| view | 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 |
| view | 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 | a0001c0001t0005 a0001c0001t0018 |
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 | a0001c0001t0019 a0001c0001t0020 |
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 | a0001c0001t0012 a0001c0001t0033 |
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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0018 |
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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(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 | a0001c0001t0008 a0001c0001t0010 |
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 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0019 others(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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(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 | a0001c0001t0011 a0001c0001t0030 |
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 |
| view | 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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
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 | 7 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0001g0246 others(4): Show |
7 | HG02622.hp2 HG02965.hp2 NA18522.hp2 others(4): 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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0239 others(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 | a0001c0001t0006g0243 a0001c0001t0014g0217 |
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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | a0001c0001t0002g0159 a0001c0001t0017g0160 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(148): 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 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(74): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): 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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0003g0181 a0001c0001t0003g0216 a0001c0001t0006g0243 others(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 | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(81): Show |
84 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(81): 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 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0113 a0001c0001t0003g0085 |
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 | a0001c0001t0001g0200 a0001c0001t0001g0213 a0001c0001t0012g0212 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0029 others(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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(131): 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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0014g0171 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0239 a0001c0001t0007g0236 a0001c0001t0007g0237 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0014g0171 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0003g0181 a0001c0001t0003g0216 a0001c0001t0006g0243 others(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 | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
117 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(114): 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 | a0001c0001t0001g0239 a0001c0001t0002g0159 a0001c0001t0002g0219 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0003g0181 a0001c0001t0003g0216 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(6): Show |
9 | HG01433.hp2 HG01516.hp2 HG02258.hp1 others(6): 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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0014g0171 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
163 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(160): 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 | a0001c0001t0001g0178 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(147): 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 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0111 a0001c0001t0003g0081 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(84): Show |
87 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.27+9494C>T | NFIX | ENSG00000008441.19 | transcript | ENST00000592199.6 | protein_coding | 1/10 | chr19 | 13005358 | |||||||
| chr19:13005428 | C | T | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(81): Show |
84 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(81): 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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0014g0171 others(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 | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(83): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0018 a0001c0001t0005g0126 a0001c0001t0027g0170 |
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 | a0001c0001t0001g0018 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0242 |
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 | a0001c0001t0002g0235 a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0007g0236 a0001c0001t0007g0237 a0001c0001t0007g0238 |
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 | a0001c0001t0001g0247 a0001c0001t0032g0157 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0079 others(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 | a0001c0001t0004g0017 a0001c0001t0004g0091 a0001c0001t0004g0092 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0005g0120 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 |
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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 |
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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
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 | a0001c0001t0007g0236 a0001c0001t0007g0237 a0001c0001t0007g0238 |
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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | 108 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(105): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(105): 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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0072 a0001c0001t0001g0086 others(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 | a0001c0001t0008g0201 a0001c0001t0008g0209 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0068 a0001c0001t0001g0070 others(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 | 72 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(69): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0175 a0001c0001t0003g0174 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0066 a0001c0001t0029g0116 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0003g0177 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0087 a0001c0001t0001g0097 others(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 | a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0197 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0003g0177 a0001c0001t0032g0157 a0001c0001t0035g0180 |
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 | a0001c0001t0001g0213 a0001c0001t0001g0247 a0001c0001t0012g0212 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0152 a0001c0001t0014g0171 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0218 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0087 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0084 a0001c0001t0001g0175 others(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 | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): 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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0067 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0024 others(96): Show |
99 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(96): 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 | a0001c0001t0001g0076 a0001c0001t0003g0085 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0247 a0001c0001t0002g0228 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0213 a0001c0001t0009g0010 a0001c0001t0011g0252 others(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 | a0001c0001t0001g0124 a0001c0001t0003g0181 a0001c0001t0005g0120 others(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 | a0001c0001t0003g0216 a0001c0001t0009g0007 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0109 a0001c0001t0001g0178 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0146 a0001c0001t0001g0165 others(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 | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0057 others(20): Show |
23 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(20): 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 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0003g0174 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0176 a0001c0001t0002g0128 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0247 a0001c0001t0003g0081 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0008g0006 others(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 | a0001c0001t0001g0178 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0003g0174 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0124 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0213 a0001c0001t0006g0168 a0001c0001t0006g0182 others(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 | a0001c0001t0006g0153 a0001c0001t0019g0211 |
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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0192 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0197 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0062 a0001c0001t0026g0046 |
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 | a0001c0001t0001g0141 a0001c0001t0012g0214 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0074 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0056 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0002t0001g0019 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0124 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 |
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 | a0001c0001t0001g0176 a0001c0001t0003g0162 a0001c0001t0017g0160 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0164 a0001c0001t0003g0177 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0151 a0001c0001t0001g0175 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0006g0153 a0001c0001t0019g0211 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0027 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0076 a0001c0001t0021g0172 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0002g0230 a0001c0001t0010g0229 |
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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0149 a0001c0001t0030g0169 |
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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0067 others(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 | a0001c0001t0013g0227 a0001c0001t0013g0231 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0154 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0015g0134 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0249 a0001c0001t0001g0250 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0079 a0001c0001t0027g0170 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0008g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0146 a0001c0001t0001g0165 |
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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0004g0017 a0001c0001t0004g0091 a0001c0001t0004g0092 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0007g0236 a0001c0001t0007g0237 a0001c0001t0007g0238 |
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 | a0001c0001t0006g0153 a0001c0001t0019g0211 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0012 a0001c0001t0036g0011 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0027 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0242 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0213 a0001c0001t0012g0212 a0001c0001t0012g0214 others(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 | |||||||
| chr19:13054718 | G | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0062 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0233 |
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 | a0001c0001t0004g0017 a0001c0001t0004g0091 a0001c0001t0004g0092 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0006g0153 a0001c0001t0019g0211 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0247 a0001c0001t0011g0251 a0001c0001t0011g0252 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0107 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0105 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0076 a0001c0001t0002g0128 a0001c0001t0002g0135 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | 233 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): 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 | a0001c0001t0001g0197 a0001c0001t0001g0210 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | |||||||
| chr19:13065046 | T | TC | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): 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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0192 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): 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 | a0001c0001t0014g0171 a0001c0001t0014g0217 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0143 a0001c0001t0008g0209 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0071 a0001c0001t0002g0235 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0071 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0210 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0008g0201 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0022g0088 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
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 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0216 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0146 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0012 a0001c0001t0036g0011 |
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 | a0001c0001t0014g0171 a0001c0001t0014g0217 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0045 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0006g0153 a0001c0001t0019g0211 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0154 a0001c0001t0019g0211 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 a0001c0001t0024g0119 |
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 | a0001c0001t0002g0159 a0001c0001t0002g0219 a0001c0001t0002g0220 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(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 | a0001c0001t0001g0247 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0177 a0001c0001t0003g0179 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0002t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0203 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0070 a0001c0001t0011g0251 a0001c0001t0011g0252 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0002g0230 a0001c0001t0010g0229 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0247 a0001c0001t0017g0160 a0001c0001t0020g0244 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0191 others(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 | a0001c0001t0002g0220 a0001c0001t0006g0153 |
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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0026 a0001c0002t0001g0019 a0001c0002t0001g0080 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0015g0134 |
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 | a0001c0001t0019g0211 a0001c0001t0020g0244 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0247 a0001c0001t0003g0081 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0087 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0108 others(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 | 16 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0079 others(13): Show |
16 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(13): 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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0243 others(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 | a0001c0001t0002g0235 a0001c0001t0007g0236 a0001c0001t0007g0237 others(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 | a0001c0001t0001g0084 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0061 others(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 | a0001c0001t0003g0085 a0001c0001t0006g0168 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0028 a0001c0001t0003g0181 a0001c0001t0003g0216 others(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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0179 |
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 | a0001c0001t0003g0085 a0001c0001t0003g0161 a0001c0001t0003g0162 others(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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0030g0169 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0011g0251 a0001c0001t0011g0252 a0001c0001t0019g0211 others(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 |