Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79023 |
|---|---|
| ensemblid | ENSG00000075188.9 |
| hgncid | 29929 |
| symbol | NUP37 |
| name | nucleoporin 37 |
| refseq_nuc | NM_024057.4 |
| refseq_prot | NP_076962.2 |
| ensembl_nuc | ENST00000552283.6 |
| ensembl_prot | ENSP00000448054.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 102073103 |
| end | 102120114 |
| strand | - |
| ver | v1.2 |
| region | chr12:102073103-102120114 |
| region5000 | chr12:102068103-102125114 |
| regionname0 | NUP37_chr12_102073103_102120114 |
| regionname5000 | NUP37_chr12_102068103_102125114 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 326 | 395 | 92 | 68 | 180 | 16 | 37 | 140 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0002 | 0/0 | 326 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0003 | 0/0 | 326 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0004 | 0/0 | 326 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 981 | 390 | 91 | 68 | 179 | 15 | 35 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0002 | 0/0 | 981 | 3 | 1 | 0 | 0 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0003 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0004 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0005 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0006 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| c0007 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1382 | 252 | 76 | 47 | 87 | 13 | 27 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0002 | 0/0 | 1380 | 73 | 1 | 13 | 54 | 0 | 5 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0003 | 0/0 | 1382 | 55 | 5 | 4 | 40 | 2 | 4 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0004 | 0/0 | 1382 | 9 | 8 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0005 | 0/0 | 1382 | 5 | 0 | 3 | 0 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0006 | 0/0 | 1382 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0007 | 0/0 | 1382 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0008 | 0/0 | 1382 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| t0009 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 18 | 1 | 3 | 12 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0002 | 0/0 | 16 | 0 | 0 | 14 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0003 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0004 | 0/0 | 10 | 0 | 2 | 1 | 4 | 3 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0005 | 0/1 | 9 | 0 | 1 | 4 | 2 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0006 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 981 | 390 | 91 | 68 | 179 | 15 | 35 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0002 | 0/0 | 981 | 3 | 1 | 0 | 0 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0006 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0007 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0002c0004 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0003c0005 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0004c0003 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2362 | 246 | 75 | 47 | 85 | 12 | 25 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0002 | 0/0 | 2360 | 72 | 1 | 13 | 53 | 0 | 5 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0003 | 0/0 | 2362 | 54 | 5 | 4 | 40 | 2 | 3 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0004 | 0/0 | 2362 | 9 | 8 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0005 | 0/0 | 2362 | 5 | 0 | 3 | 0 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0006 | 0/0 | 2362 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0007 | 0/0 | 2362 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0008 | 0/0 | 2362 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0001t0009 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0002t0001 | 0/0 | 2362 | 3 | 1 | 0 | 0 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0006t0003 | 0/0 | 2362 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0001c0007t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0002c0004t0001 | 0/0 | 2362 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0003c0005t0001 | 0/0 | 2362 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| a0004c0003t0001 | 0/0 | 2362 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | copy fasta | chr12 | 102068103 | 102125114 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 2 | 1 | 4 | 3 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0005 | 0/1 | 9 | 0 | 1 | 4 | 2 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0002 | 0/0 | 16 | 0 | 0 | 14 | 0 | 2 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0001 | 0/0 | 18 | 1 | 3 | 12 | 1 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0005g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0001t0009g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0006t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0001c0007t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0003c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| a0004c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0040 | EUR | GBR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0270 | EUR | FIN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01993 | hp2 | a0001 | c0001 | t0009 | g0237 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CDX | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CDX | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CDX | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02683 | hp1 | a0001 | c0006 | t0003 | g0211 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03688 | hp2 | a0003 | c0005 | t0001 | g0164 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0138 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0146 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CHB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18970 | hp2 | a0001 | c0007 | t0002 | g0242 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18975 | hp1 | a0004 | c0003 | t0001 | g0130 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18997 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0228 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ASW | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0206 | EUR | TSI | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | GIH | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | USA | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | USA | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0122 | REF | REF | NUP37_chr12_102068103_102125114 | NUP37 | chr12 | 102068103 | 102125114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102077365
|
C | T | 1 | a0003 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.679G>A | p.Val227Ile | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 7/10 | 809/2362 | 679/981 | 227/326 | chr12 | 102077365 | ||
| chr12:102099163
|
A | C | 1 | a0002 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.392T>G | p.Val131Gly | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/10 | 522/2362 | 392/981 | 131/326 | chr12 | 102099163 | ||
| chr12:102099182
|
C | T | 1 | a0004 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.373G>A | p.Asp125Asn | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/10 | 503/2362 | 373/981 | 125/326 | chr12 | 102099182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102074450
|
A | G | 1 | a0001c0006 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.885T>C | p.Ser295Ser | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 1015/2362 | 885/981 | 295/326 | chr12 | 102074450 | ||
| chr12:102076838
|
T | C | 1 | a0001c0007 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.732A>G | p.Gln244Gln | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/10 | 862/2362 | 732/981 | 244/326 | chr12 | 102076838 | ||
| chr12:102099162
|
C | A | 1 | a0002c0004 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.393G>T | p.Val131Val | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/10 | 523/2362 | 393/981 | 131/326 | chr12 | 102099162 | ||
| chr12:102101071
|
T | C | 1 | a0001c0002 | 3 | HG00323.hp1 HG02559.hp1 HG04115.hp2 |
synonymous_variant | LOW | c.315A>G | p.Arg105Arg | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/10 | 445/2362 | 315/981 | 105/326 | chr12 | 102101071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102073214
|
T | C | 2 | a0001c0001t0003a0001c0006t0003 | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1140A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 1140 | chr12 | 102073214 | |||||
| chr12:102073546
|
C | T | 1 | a0001c0001t0004 | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 808 | chr12 | 102073546 | |||||
| chr12:102073560
|
G | C | 1 | a0001c0001t0009 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*794C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 794 | chr12 | 102073560 | |||||
| chr12:102073747
|
C | T | 1 | a0001c0001t0008 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 607 | chr12 | 102073747 | |||||
| chr12:102073926
|
C | T | 1 | a0001c0001t0007 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 428 | chr12 | 102073926 | |||||
| chr12:102074163
|
C | T | 1 | a0001c0001t0005 | 5 | HG00642.hp2 HG01106.hp2 HG01109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*191G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 191 | chr12 | 102074163 | |||||
| chr12:102074169
|
CAG | C | 3 | a0001c0001t0002a0001c0001t0009a0001c0007t0002 | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*183_*184delCT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 183 | chr12 | 102074169 | |||||
| chr12:102074171
|
G | T | 1 | a0001c0001t0006 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 10/10 | 183 | chr12 | 102074171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102074613
|
A | G | 1 | a0001c0001t0003g0214 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.868-146T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 9/9 | chr12 | 102074613 | ||||||
| chr12:102074768
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.867+233A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 9/9 | chr12 | 102074768 | ||||||
| chr12:102074831
|
C | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.867+170G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 9/9 | chr12 | 102074831 | ||||||
| chr12:102074882
|
A | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.867+119T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 9/9 | chr12 | 102074882 | ||||||
| chr12:102075163
|
GCTTTTT | G | 6 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0204others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-75_774-70delAA others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102075163 | ||||||
| chr12:102075330
|
G | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | NA18939.hp2 NA18952.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-236C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102075330 | ||||||
| chr12:102075343
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.774-249C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102075343 | ||||||
| chr12:102075412
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.774-318G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102075412 | ||||||
| chr12:102075699
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.774-605C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102075699 | ||||||
| chr12:102076064
|
T | C | 1 | a0001c0001t0001g0030 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.773+733A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076064 | ||||||
| chr12:102076178
|
C | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+619G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076178 | ||||||
| chr12:102076192
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.773+605G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076192 | ||||||
| chr12:102076261
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.773+536A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076261 | ||||||
| chr12:102076396
|
A | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(35): Show | 53 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.773+401T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076396 | ||||||
| chr12:102076417
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0227 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.773+380C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076417 | ||||||
| chr12:102076603
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.773+194C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076603 | ||||||
| chr12:102076656
|
C | T | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.773+141G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076656 | ||||||
| chr12:102076754
|
G | A | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0212others(2): Show | 5 | NA18944.hp2 NA18962.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.773+43C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 8/9 | chr12 | 102076754 | ||||||
| chr12:102076854
|
G | T | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.723-7C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 7/9 | chr12 | 102076854 | ||||||
| chr12:102076948
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.723-101T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 7/9 | chr12 | 102076948 | ||||||
| chr12:102077245
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0085others(3): Show | 8 | HG00099.hp2 HG01123.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.722+77C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 7/9 | chr12 | 102077245 | ||||||
| chr12:102077602
|
A | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-99T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102077602 | ||||||
| chr12:102077609
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.541-106T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102077609 | ||||||
| chr12:102077750
|
A | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0098others(7): Show | 11 | HG00673.hp2 HG02135.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.541-247T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102077750 | ||||||
| chr12:102077751
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541-248T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102077751 | ||||||
| chr12:102077980
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 24 | HG00099.hp2 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.541-477A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102077980 | ||||||
| chr12:102078082
|
C | T | 48 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(45): Show | 75 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.541-579G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078082 | ||||||
| chr12:102078165
|
T | TA | 9 | a0001c0001t0001g0066a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-663dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078165 | ||||||
| chr12:102078187
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.541-684G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078187 | ||||||
| chr12:102078222
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.541-719C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078222 | ||||||
| chr12:102078240
|
T | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.541-737A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078240 | ||||||
| chr12:102078322
|
T | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.541-819A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078322 | ||||||
| chr12:102078324
|
CT | C | 91 | a0001c0001t0001g0099a0001c0001t0001g0167a0001c0001t0001g0194others(88): Show | 142 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.541-822delA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078324 | ||||||
| chr12:102078327
|
T | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.541-824A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078327 | ||||||
| chr12:102078497
|
A | G | 2 | a0001c0001t0004g0201a0001c0001t0004g0222 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.541-994T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078497 | ||||||
| chr12:102078583
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.541-1080G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078583 | ||||||
| chr12:102078824
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.541-1321C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078824 | ||||||
| chr12:102078904
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-1401C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078904 | ||||||
| chr12:102078982
|
C | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.541-1479G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102078982 | ||||||
| chr12:102079025
|
T | C | 1 | a0001c0001t0003g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.541-1522A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079025 | ||||||
| chr12:102079201
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.541-1698C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079201 | ||||||
| chr12:102079318
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-1815T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079318 | ||||||
| chr12:102079331
|
T | C | 2 | a0001c0001t0003g0209a0001c0001t0003g0219 | 2 | NA18944.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.541-1828A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079331 | ||||||
| chr12:102079433
|
T | C | 1 | a0001c0001t0003g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.541-1930A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079433 | ||||||
| chr12:102079437
|
A | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.541-1934T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079437 | ||||||
| chr12:102079438
|
A | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.541-1935T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079438 | ||||||
| chr12:102079518
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.541-2015G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079518 | ||||||
| chr12:102079720
|
GATTTTAC others(8): Show |
G | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-2232_541-2218d others(17): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079720 | ||||||
| chr12:102079929
|
T | C | 3 | a0001c0001t0004g0049a0001c0001t0004g0204a0001c0001t0004g0205 | 3 | HG02451.hp2 HG02486.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.541-2426A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102079929 | ||||||
| chr12:102080052
|
C | T | 1 | a0001c0001t0005g0138 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.541-2549G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080052 | ||||||
| chr12:102080140
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0166 | 4 | HG01243.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-2637A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080140 | ||||||
| chr12:102080141
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.541-2638T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080141 | ||||||
| chr12:102080158
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-2655A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080158 | ||||||
| chr12:102080317
|
G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0142 | 5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2814C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080317 | ||||||
| chr12:102080414
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.541-2911G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080414 | ||||||
| chr12:102080459
|
G | A | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.541-2956C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080459 | ||||||
| chr12:102080733
|
C | G | 1 | a0001c0001t0001g0022 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.541-3230G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080733 | ||||||
| chr12:102080757
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.541-3254A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080757 | ||||||
| chr12:102080790
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.541-3287C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080790 | ||||||
| chr12:102080943
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0175 | 3 | HG02486.hp2 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.541-3440A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080943 | ||||||
| chr12:102080954
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0167 | 2 | HG02683.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.541-3451G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102080954 | ||||||
| chr12:102081071
|
C | T | 40 | a0001c0001t0001g0136a0001c0001t0002g0002a0001c0001t0002g0007others(37): Show | 66 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.541-3568G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081071 | ||||||
| chr12:102081074
|
C | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.541-3571G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081074 | ||||||
| chr12:102081232
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | NA18970.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.541-3729A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081232 | ||||||
| chr12:102081341
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0030others(8): Show | 15 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-3838A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081341 | ||||||
| chr12:102081411
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0102 | 3 | NA18969.hp2 NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.541-3908T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081411 | ||||||
| chr12:102081530
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0056others(4): Show | 9 | HG00621.hp2 HG02040.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-4027C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081530 | ||||||
| chr12:102081585
|
A | C | 1 | a0001c0001t0002g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.541-4082T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081585 | ||||||
| chr12:102081662
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.540+4104C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081662 | ||||||
| chr12:102081715
|
A | AT | 7 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0066others(4): Show | 8 | HG01167.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+4050dupA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081715 | ||||||
| chr12:102081834
|
C | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0236a0001c0001t0002g0241others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+3932G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081834 | ||||||
| chr12:102081918
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0115 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.540+3848G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102081918 | ||||||
| chr12:102082074
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.540+3692C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082074 | ||||||
| chr12:102082112
|
T | C | 1 | a0001c0007t0002g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.540+3654A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082112 | ||||||
| chr12:102082240
|
C | CT | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+3525dupA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082240 | ||||||
| chr12:102082309
|
A | C | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.540+3457T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082309 | ||||||
| chr12:102082350
|
A | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.540+3416T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082350 | ||||||
| chr12:102082439
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0246 | 3 | NA18952.hp1 NA18956.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.540+3327C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082439 | ||||||
| chr12:102082461
|
C | CAATAATA others(322): Show |
1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.540+3304_540+3305i others(331): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082461 | ||||||
| chr12:102082605
|
T | C | 3 | a0001c0001t0003g0042a0001c0001t0003g0214a0001c0001t0003g0217 | 4 | NA18948.hp2 NA18964.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+3161A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082605 | ||||||
| chr12:102082625
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.540+3141C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082625 | ||||||
| chr12:102082651
|
C | T | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.540+3115G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082651 | ||||||
| chr12:102082799
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.540+2967C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102082799 | ||||||
| chr12:102083088
|
G | T | 1 | a0001c0001t0001g0025 | 2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.540+2678C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083088 | ||||||
| chr12:102083277
|
G | T | 1 | a0001c0002t0001g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+2489C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083277 | ||||||
| chr12:102083369
|
T | G | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+2397A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083369 | ||||||
| chr12:102083378
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.540+2388C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083378 | ||||||
| chr12:102083409
|
A | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(36): Show | 56 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.540+2357T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083409 | ||||||
| chr12:102083795
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.540+1971T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083795 | ||||||
| chr12:102083931
|
T | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(8): Show | 12 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.540+1835A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102083931 | ||||||
| chr12:102084160
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.540+1606G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084160 | ||||||
| chr12:102084282
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.540+1484G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084282 | ||||||
| chr12:102084470
|
A | ACT | 124 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(121): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.540+1294_540+1295d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084470 | ||||||
| chr12:102084473
|
G | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0197a0001c0001t0003g0198others(1): Show | 6 | NA18942.hp1 NA18955.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1293C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084473 | ||||||
| chr12:102084581
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.540+1185A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084581 | ||||||
| chr12:102084615
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.540+1151T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084615 | ||||||
| chr12:102084708
|
CA | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG01167.hp2 HG01515.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1057delT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084708 | ||||||
| chr12:102084741
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0079 | 3 | HG00544.hp2 HG02071.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.540+1025C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084741 | ||||||
| chr12:102084916
|
T | C | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.540+850A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084916 | ||||||
| chr12:102084971
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+795C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102084971 | ||||||
| chr12:102085044
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.540+722T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085044 | ||||||
| chr12:102085102
|
CAACA | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0123others(1): Show | 4 | HG02717.hp2 HG03516.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+660_540+663del others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085102 | ||||||
| chr12:102085254
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0142 | 5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+512A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085254 | ||||||
| chr12:102085403
|
C | T | 1 | a0001c0006t0003g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.540+363G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085403 | ||||||
| chr12:102085501
|
A | G | 4 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0244others(1): Show | 4 | HG02135.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+265T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085501 | ||||||
| chr12:102085561
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+205T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085561 | ||||||
| chr12:102085580
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.540+186A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085580 | ||||||
| chr12:102085689
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+77G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085689 | ||||||
| chr12:102085712
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.540+54T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 6/9 | chr12 | 102085712 | ||||||
| chr12:102085885
|
AT | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0161others(1): Show | 5 | NA18939.hp1 NA18942.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-30delA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102085885 | ||||||
| chr12:102085986
|
C | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0220 | 3 | HG00597.hp2 NA18993.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.450-130G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102085986 | ||||||
| chr12:102086071
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.450-215C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086071 | ||||||
| chr12:102086145
|
T | C | 8 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.450-289A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086145 | ||||||
| chr12:102086250
|
G | A | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.450-394C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086250 | ||||||
| chr12:102086425
|
T | C | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-569A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086425 | ||||||
| chr12:102086609
|
G | A | 1 | a0001c0001t0003g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.450-753C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086609 | ||||||
| chr12:102086622
|
A | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0123others(1): Show | 4 | HG02717.hp2 HG03516.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-766T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086622 | ||||||
| chr12:102086645
|
C | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(36): Show | 65 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.450-789G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086645 | ||||||
| chr12:102086899
|
T | G | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-1043A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102086899 | ||||||
| chr12:102087027
|
G | C | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-1171C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087027 | ||||||
| chr12:102087050
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.450-1194G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087050 | ||||||
| chr12:102087149
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0229 | 5 | HG00609.hp1 HG00673.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.450-1293C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087149 | ||||||
| chr12:102087274
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0182others(11): Show | 18 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.450-1418A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087274 | ||||||
| chr12:102087295
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.450-1439G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087295 | ||||||
| chr12:102087676
|
T | C | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-1820A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087676 | ||||||
| chr12:102087678
|
G | A | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-1822C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087678 | ||||||
| chr12:102087886
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.450-2030C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087886 | ||||||
| chr12:102087936
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.450-2080A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102087936 | ||||||
| chr12:102088396
|
C | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0138a0001c0001t0005g0145others(1): Show | 5 | HG00642.hp2 HG01106.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.450-2540G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088396 | ||||||
| chr12:102088692
|
TTTTTG | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 17 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.450-2841_450-2837d others(7): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088692 | ||||||
| chr12:102088703
|
AT | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0161a0001c0001t0001g0167others(4): Show | 8 | HG00099.hp1 HG01070.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.450-2848delA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088703 | ||||||
| chr12:102088708
|
T | TC | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.450-2853_450-2852i others(3): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088708 | ||||||
| chr12:102088755
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.450-2899C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088755 | ||||||
| chr12:102088787
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.450-2931A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088787 | ||||||
| chr12:102088836
|
T | TTCCTAGG others(6): Show |
1 | a0001c0001t0001g0011 | 3 | HG01884.hp2 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.450-2993_450-2981d others(15): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102088836 | ||||||
| chr12:102089040
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.450-3184A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089040 | ||||||
| chr12:102089046
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450-3190G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089046 | ||||||
| chr12:102089190
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.450-3334C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089190 | ||||||
| chr12:102089197
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0189a0001c0001t0006g0188 | 6 | HG02647.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.450-3341A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089197 | ||||||
| chr12:102089216
|
G | A | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-3360C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089216 | ||||||
| chr12:102089295
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.450-3439C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089295 | ||||||
| chr12:102089299
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.450-3443G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089299 | ||||||
| chr12:102089317
|
C | CG | 17 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(14): Show | 17 | HG01071.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.450-3462dupC | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089317 | ||||||
| chr12:102089317
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.450-3461G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089317 | ||||||
| chr12:102089318
|
GGGGTGGC others(33): Show |
G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.450-3502_450-3463d others(42): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089318 | ||||||
| chr12:102089337
|
G | C | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0274others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-3481C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089337 | ||||||
| chr12:102089397
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.450-3541G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089397 | ||||||
| chr12:102089398
|
G | A | 1 | a0001c0001t0003g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.450-3542C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089398 | ||||||
| chr12:102089452
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.450-3596G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089452 | ||||||
| chr12:102089454
|
G | A | 2 | a0001c0001t0004g0202a0001c0001t0004g0203 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.450-3598C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089454 | ||||||
| chr12:102089462
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450-3606C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089462 | ||||||
| chr12:102089471
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.450-3615G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089471 | ||||||
| chr12:102089474
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.450-3618A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089474 | ||||||
| chr12:102089489
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.450-3633G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089489 | ||||||
| chr12:102089495
|
A | G | 96 | a0001c0001t0001g0227a0001c0001t0001g0271a0001c0001t0001g0272others(93): Show | 147 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.450-3639T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089495 | ||||||
| chr12:102089566
|
G | A | 2 | a0001c0001t0002g0262a0001c0001t0002g0266 | 2 | NA18953.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.450-3710C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089566 | ||||||
| chr12:102089621
|
C | T | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-3765G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089621 | ||||||
| chr12:102089660
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG01070.hp2 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-3804G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089660 | ||||||
| chr12:102089662
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.450-3806G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089662 | ||||||
| chr12:102089676
|
G | C | 2 | a0001c0001t0003g0041a0001c0001t0003g0220 | 3 | HG00597.hp2 NA18993.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.450-3820C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089676 | ||||||
| chr12:102089687
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.450-3831G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089687 | ||||||
| chr12:102089716
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.450-3860C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089716 | ||||||
| chr12:102089721
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.450-3865C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089721 | ||||||
| chr12:102089806
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0090a0001c0001t0001g0093others(5): Show | 9 | HG02717.hp2 HG03516.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-3950C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089806 | ||||||
| chr12:102089914
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.450-4058C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102089914 | ||||||
| chr12:102090016
|
A | G | 2 | a0001c0001t0004g0201a0001c0001t0004g0222 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.450-4160T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090016 | ||||||
| chr12:102090044
|
G | C | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.450-4188C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090044 | ||||||
| chr12:102090100
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.450-4244A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090100 | ||||||
| chr12:102090301
|
T | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.450-4445A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090301 | ||||||
| chr12:102090334
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.450-4478T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090334 | ||||||
| chr12:102090412
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.450-4556A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090412 | ||||||
| chr12:102090604
|
G | GA | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG01070.hp2 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-4749dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090604 | ||||||
| chr12:102090876
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.450-5020C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090876 | ||||||
| chr12:102090914
|
T | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(8): Show | 12 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.450-5058A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090914 | ||||||
| chr12:102090937
|
C | G | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-5081G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102090937 | ||||||
| chr12:102091158
|
A | T | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-5302T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091158 | ||||||
| chr12:102091395
|
G | A | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450-5539C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091395 | ||||||
| chr12:102091399
|
C | CA | 69 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0014others(66): Show | 84 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.450-5544dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
C | CAA | 6 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01884.hp1 HG01928.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-5545_450-5544d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
CA | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0094others(2): Show | 6 | HG01070.hp2 NA18939.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.450-5544delT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
CAAAAA | C | 18 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(15): Show | 20 | HG01978.hp2 HG02080.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.450-5548_450-5544d others(7): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
CAAAAAA | C | 34 | a0001c0001t0002g0045a0001c0001t0002g0232a0001c0001t0002g0243others(31): Show | 57 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.450-5549_450-5544d others(8): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
CAAAAAAA | C | 30 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(27): Show | 56 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.450-5550_450-5544d others(9): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091399
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.450-5556_450-5544d others(15): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091399 | ||||||
| chr12:102091416
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.450-5560T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091416 | ||||||
| chr12:102091612
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.450-5756A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091612 | ||||||
| chr12:102091956
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0078 | 4 | HG00621.hp2 HG02074.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-6100C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102091956 | ||||||
| chr12:102092130
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.450-6274A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102092130 | ||||||
| chr12:102092163
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0251a0001c0001t0007g0228 | 7 | NA18948.hp1 NA18957.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.450-6307A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102092163 | ||||||
| chr12:102092459
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.450-6603C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102092459 | ||||||
| chr12:102092847
|
T | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | HG02258.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.449+6259A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102092847 | ||||||
| chr12:102093045
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.449+6061T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102093045 | ||||||
| chr12:102093126
|
A | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+5980T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102093126 | ||||||
| chr12:102093129
|
C | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0258a0001c0001t0002g0259 | 4 | HG01257.hp2 HG01258.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.449+5977G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102093129 | ||||||
| chr12:102093260
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01167.hp2 HG01169.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.449+5846C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102093260 | ||||||
| chr12:102093490
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.449+5616G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102093490 | ||||||
| chr12:102094044
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.449+5062T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094044 | ||||||
| chr12:102094064
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.449+5042T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094064 | ||||||
| chr12:102094383
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+4723C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094383 | ||||||
| chr12:102094515
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+4591C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094515 | ||||||
| chr12:102094721
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.449+4385C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094721 | ||||||
| chr12:102094965
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.449+4141C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102094965 | ||||||
| chr12:102095111
|
T | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.449+3995A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102095111 | ||||||
| chr12:102095441
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.449+3665A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102095441 | ||||||
| chr12:102095476
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449+3630G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102095476 | ||||||
| chr12:102095524
|
A | G | 89 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(86): Show | 140 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.449+3582T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102095524 | ||||||
| chr12:102096153
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0189a0001c0001t0006g0188 | 6 | HG02647.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.449+2953T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096153 | ||||||
| chr12:102096441
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.449+2665G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096441 | ||||||
| chr12:102096589
|
TTAAG | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0182others(10): Show | 17 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.449+2513_449+2516d others(6): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096589 | ||||||
| chr12:102096611
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.449+2495G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096611 | ||||||
| chr12:102096686
|
A | C | 48 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(45): Show | 75 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.449+2420T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096686 | ||||||
| chr12:102096777
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.449+2329A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096777 | ||||||
| chr12:102096834
|
C | A | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.449+2272G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096834 | ||||||
| chr12:102096848
|
G | A | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.449+2258C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096848 | ||||||
| chr12:102096860
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.449+2246C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102096860 | ||||||
| chr12:102097132
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.449+1974C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097132 | ||||||
| chr12:102097460
|
T | TAA | 89 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(86): Show | 140 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.449+1644_449+1645d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097460 | ||||||
| chr12:102097523
|
G | T | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.449+1583C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097523 | ||||||
| chr12:102097563
|
AAAAC | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035others(26): Show | 43 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.449+1539_449+1542d others(6): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097563 | ||||||
| chr12:102097689
|
T | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.449+1417A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097689 | ||||||
| chr12:102097730
|
C | A | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.449+1376G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097730 | ||||||
| chr12:102097738
|
C | T | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.449+1368G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097738 | ||||||
| chr12:102097739
|
C | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.449+1367G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097739 | ||||||
| chr12:102097864
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449+1242A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102097864 | ||||||
| chr12:102098176
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.449+930G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098176 | ||||||
| chr12:102098205
|
C | T | 41 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(38): Show | 65 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.449+901G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098205 | ||||||
| chr12:102098213
|
C | T | 1 | a0001c0001t0003g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.449+893G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098213 | ||||||
| chr12:102098235
|
T | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.449+871A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098235 | ||||||
| chr12:102098272
|
A | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+834T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098272 | ||||||
| chr12:102098313
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.449+793C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098313 | ||||||
| chr12:102098403
|
T | C | 1 | a0001c0001t0003g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.449+703A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098403 | ||||||
| chr12:102098432
|
T | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.449+674A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098432 | ||||||
| chr12:102098446
|
T | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+660A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098446 | ||||||
| chr12:102098449
|
T | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+657A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098449 | ||||||
| chr12:102098649
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.449+457T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098649 | ||||||
| chr12:102098678
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(4): Show | 10 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.449+428G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098678 | ||||||
| chr12:102098687
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.449+419C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098687 | ||||||
| chr12:102098728
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.449+378G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098728 | ||||||
| chr12:102098780
|
C | T | 89 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(86): Show | 140 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.449+326G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098780 | ||||||
| chr12:102098812
|
A | G | 178 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(175): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.449+294T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102098812 | ||||||
| chr12:102099027
|
A | T | 1 | a0002c0004t0001g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.449+79T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102099027 | ||||||
| chr12:102099076
|
A | C | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.449+30T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 5/9 | chr12 | 102099076 | ||||||
| chr12:102099424
|
T | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01175.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.355-224A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099424 | ||||||
| chr12:102099455
|
AAC | A | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.355-257_355-256del others(2): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099455 | ||||||
| chr12:102099633
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.355-433G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099633 | ||||||
| chr12:102099637
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0059 | 3 | HG02040.hp2 NA18747.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.355-437G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099637 | ||||||
| chr12:102099720
|
C | T | 1 | a0001c0001t0001g0011 | 3 | HG01884.hp2 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.355-520G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099720 | ||||||
| chr12:102099990
|
A | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.355-790T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102099990 | ||||||
| chr12:102100036
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.355-836G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100036 | ||||||
| chr12:102100157
|
T | A | 1 | a0002c0004t0001g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.354+875A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100157 | ||||||
| chr12:102100218
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.354+814G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100218 | ||||||
| chr12:102100430
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.354+602G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100430 | ||||||
| chr12:102100650
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.354+382G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100650 | ||||||
| chr12:102100678
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.354+354C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100678 | ||||||
| chr12:102100811
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.354+221T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100811 | ||||||
| chr12:102100869
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.354+163T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 4/9 | chr12 | 102100869 | ||||||
| chr12:102101353
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.282-249A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102101353 | ||||||
| chr12:102101444
|
A | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.282-340T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102101444 | ||||||
| chr12:102101555
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.282-451G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102101555 | ||||||
| chr12:102101606
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282-502A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102101606 | ||||||
| chr12:102101967
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0092others(5): Show | 11 | HG01069.hp1 HG01243.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-863G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102101967 | ||||||
| chr12:102102407
|
T | G | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282-1303A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102102407 | ||||||
| chr12:102103043
|
CT | C | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.282-1940delA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103043 | ||||||
| chr12:102103098
|
A | C | 1 | a0001c0002t0001g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.282-1994T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103098 | ||||||
| chr12:102103289
|
C | T | 8 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG00673.hp2 HG02135.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-2185G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103289 | ||||||
| chr12:102103365
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.282-2261A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103365 | ||||||
| chr12:102103409
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.282-2305T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103409 | ||||||
| chr12:102103450
|
T | C | 1 | a0001c0001t0003g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.282-2346A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103450 | ||||||
| chr12:102103591
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.282-2487A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103591 | ||||||
| chr12:102103671
|
A | G | 1 | a0001c0001t0002g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.282-2567T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103671 | ||||||
| chr12:102103672
|
C | A | 2 | a0001c0001t0004g0204a0001c0001t0004g0205 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.282-2568G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103672 | ||||||
| chr12:102103795
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-2691T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103795 | ||||||
| chr12:102103862
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0270 | 2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.282-2758G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103862 | ||||||
| chr12:102103875
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.282-2771T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103875 | ||||||
| chr12:102103888
|
C | T | 1 | a0001c0001t0001g0022 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.282-2784G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103888 | ||||||
| chr12:102103920
|
A | G | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.282-2816T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102103920 | ||||||
| chr12:102104113
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282-3009G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102104113 | ||||||
| chr12:102104199
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282-3095C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102104199 | ||||||
| chr12:102104639
|
T | C | 1 | a0001c0001t0002g0266 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282-3535A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102104639 | ||||||
| chr12:102104857
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0227 | 2 | HG00609.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.282-3753G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102104857 | ||||||
| chr12:102105113
|
A | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-4009T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105113 | ||||||
| chr12:102105254
|
A | G | 96 | a0001c0001t0001g0227a0001c0001t0001g0271a0001c0001t0001g0272others(93): Show | 147 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.282-4150T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105254 | ||||||
| chr12:102105255
|
T | C | 3 | a0001c0001t0004g0201a0001c0001t0004g0206a0001c0001t0004g0222 | 3 | HG02109.hp2 HG02818.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.282-4151A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105255 | ||||||
| chr12:102105318
|
C | T | 1 | a0001c0001t0003g0209 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.282-4214G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105318 | ||||||
| chr12:102105319
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.282-4215C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105319 | ||||||
| chr12:102105678
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.282-4574G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105678 | ||||||
| chr12:102105681
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282-4577G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105681 | ||||||
| chr12:102105682
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-4578C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105682 | ||||||
| chr12:102105772
|
G | T | 1 | a0004c0003t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.282-4668C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105772 | ||||||
| chr12:102105850
|
G | A | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.282-4746C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105850 | ||||||
| chr12:102105861
|
C | CA | 69 | a0001c0001t0001g0076a0001c0001t0001g0119a0001c0001t0001g0120others(66): Show | 118 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.282-4758dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105861 | ||||||
| chr12:102105861
|
C | CAA | 8 | a0001c0001t0002g0230a0001c0001t0002g0253a0001c0001t0002g0254others(5): Show | 9 | HG01361.hp2 HG01934.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.282-4759_282-4758d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105861 | ||||||
| chr12:102105861
|
CA | C | 12 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | HG00280.hp2 HG01256.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-4758delT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105861 | ||||||
| chr12:102105861
|
CAAAAAAA | C | 8 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-4764_282-4758d others(9): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105861 | ||||||
| chr12:102105907
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.282-4803A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102105907 | ||||||
| chr12:102106029
|
A | C | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282-4925T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102106029 | ||||||
| chr12:102106038
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.282-4934T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102106038 | ||||||
| chr12:102106039
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.282-4935T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102106039 | ||||||
| chr12:102106095
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.282-4991G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102106095 | ||||||
| chr12:102106681
|
A | C | 1 | a0001c0001t0004g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.281+5427T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102106681 | ||||||
| chr12:102107250
|
C | A | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+4858G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107250 | ||||||
| chr12:102107290
|
G | A | 26 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(23): Show | 50 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.281+4818C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107290 | ||||||
| chr12:102107303
|
A | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0259 | 3 | HG01257.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.281+4805T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107303 | ||||||
| chr12:102107394
|
C | T | 1 | a0001c0001t0004g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.281+4714G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107394 | ||||||
| chr12:102107678
|
A | C | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+4430T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107678 | ||||||
| chr12:102107688
|
C | A | 1 | a0001c0001t0001g0077 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.281+4420G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107688 | ||||||
| chr12:102107942
|
C | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.281+4166G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107942 | ||||||
| chr12:102107984
|
T | A | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.281+4124A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102107984 | ||||||
| chr12:102108011
|
T | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0229 | 7 | HG00609.hp1 HG00673.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+4097A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108011 | ||||||
| chr12:102108065
|
T | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0080a0001c0001t0001g0081 | 4 | HG02257.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+4043A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108065 | ||||||
| chr12:102108098
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+4010C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108098 | ||||||
| chr12:102108305
|
TA | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.281+3802delT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108305 | ||||||
| chr12:102108563
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.281+3545T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108563 | ||||||
| chr12:102108627
|
GTATGT | G | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+3476_281+3480d others(7): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108627 | ||||||
| chr12:102108648
|
C | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0123others(1): Show | 4 | HG02717.hp2 HG03516.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+3460G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108648 | ||||||
| chr12:102108668
|
CTG | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 5 | NA18968.hp1 NA18978.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+3438_281+3439d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108668 | ||||||
| chr12:102108757
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.281+3351T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108757 | ||||||
| chr12:102108810
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.281+3298C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108810 | ||||||
| chr12:102108846
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.281+3262G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108846 | ||||||
| chr12:102108981
|
T | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(237): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.281+3127A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102108981 | ||||||
| chr12:102109186
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.281+2922A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102109186 | ||||||
| chr12:102109211
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.281+2897G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102109211 | ||||||
| chr12:102109321
|
A | T | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.281+2787T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102109321 | ||||||
| chr12:102109423
|
C | T | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.281+2685G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102109423 | ||||||
| chr12:102109800
|
AAGCATAG others(8): Show |
A | 4 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0161others(1): Show | 5 | NA18939.hp1 NA18942.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+2293_281+2307d others(17): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102109800 | ||||||
| chr12:102110086
|
T | C | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.281+2022A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110086 | ||||||
| chr12:102110143
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.281+1965T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110143 | ||||||
| chr12:102110215
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281+1893T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110215 | ||||||
| chr12:102110263
|
G | A | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.281+1845C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110263 | ||||||
| chr12:102110374
|
G | A | 1 | a0001c0001t0002g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.281+1734C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110374 | ||||||
| chr12:102110434
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+1674C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110434 | ||||||
| chr12:102110515
|
TA | T | 97 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0092others(94): Show | 148 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.281+1592delT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110515 | ||||||
| chr12:102110590
|
C | A | 1 | a0001c0001t0002g0257 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281+1518G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110590 | ||||||
| chr12:102110621
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.281+1487A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110621 | ||||||
| chr12:102110623
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281+1485C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110623 | ||||||
| chr12:102110684
|
A | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+1424T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110684 | ||||||
| chr12:102110714
|
C | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+1394G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110714 | ||||||
| chr12:102110715
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+1393C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110715 | ||||||
| chr12:102110845
|
A | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(41): Show | 70 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.281+1263T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102110845 | ||||||
| chr12:102111182
|
A | C | 1 | a0001c0001t0004g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.281+926T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111182 | ||||||
| chr12:102111301
|
T | A | 1 | a0001c0001t0002g0260 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.281+807A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111301 | ||||||
| chr12:102111301
|
T | C | 1 | a0001c0001t0003g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281+807A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111301 | ||||||
| chr12:102111375
|
C | T | 107 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(104): Show | 159 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.281+733G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111375 | ||||||
| chr12:102111459
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281+649C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111459 | ||||||
| chr12:102111582
|
C | T | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+526G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111582 | ||||||
| chr12:102111795
|
A | AAG | 123 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.281+311_281+312dup others(2): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111795 | ||||||
| chr12:102111825
|
A | G | 31 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(28): Show | 55 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.281+283T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 3/9 | chr12 | 102111825 | ||||||
| chr12:102112266
|
T | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.157-34A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112266 | ||||||
| chr12:102112342
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.157-110A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112342 | ||||||
| chr12:102112498
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.157-266T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112498 | ||||||
| chr12:102112542
|
A | G | 9 | a0001c0001t0004g0049a0001c0001t0004g0201a0001c0001t0004g0202others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-310T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112542 | ||||||
| chr12:102112556
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-324G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112556 | ||||||
| chr12:102112569
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157-337C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112569 | ||||||
| chr12:102112730
|
T | TA | 10 | a0001c0001t0002g0007a0001c0001t0002g0230a0001c0001t0002g0261others(7): Show | 15 | HG00621.hp1 HG01975.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-499dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112730 | ||||||
| chr12:102112848
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02622.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.157-616A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112848 | ||||||
| chr12:102112850
|
T | C | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.157-618A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102112850 | ||||||
| chr12:102113024
|
C | T | 123 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.157-792G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113024 | ||||||
| chr12:102113116
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157-884A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113116 | ||||||
| chr12:102113239
|
C | A | 1 | a0003c0005t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.157-1007G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113239 | ||||||
| chr12:102113323
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-1091G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113323 | ||||||
| chr12:102113402
|
T | G | 2 | a0001c0001t0004g0201a0001c0001t0004g0222 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.157-1170A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113402 | ||||||
| chr12:102113752
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0270 | 2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.157-1520G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102113752 | ||||||
| chr12:102114131
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.157-1899T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114131 | ||||||
| chr12:102114257
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.157-2025A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114257 | ||||||
| chr12:102114360
|
AC | A | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.157-2129delG | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114360 | ||||||
| chr12:102114531
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-2299A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114531 | ||||||
| chr12:102114563
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.157-2331A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114563 | ||||||
| chr12:102114627
|
G | C | 1 | a0001c0001t0004g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.157-2395C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114627 | ||||||
| chr12:102114766
|
G | GTTTACA | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-2540_157-2535d others(8): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114766 | ||||||
| chr12:102114822
|
G | C | 1 | a0001c0001t0003g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.157-2590C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114822 | ||||||
| chr12:102114888
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0166 | 4 | HG01243.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-2656C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102114888 | ||||||
| chr12:102115007
|
T | C | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.157-2775A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115007 | ||||||
| chr12:102115067
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.157-2835A>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115067 | ||||||
| chr12:102115317
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+3046C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115317 | ||||||
| chr12:102115391
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156+2972T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115391 | ||||||
| chr12:102115462
|
A | C | 2 | a0001c0001t0004g0202a0001c0001t0004g0203 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.156+2901T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115462 | ||||||
| chr12:102115529
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+2834T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115529 | ||||||
| chr12:102115617
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.156+2746G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115617 | ||||||
| chr12:102115623
|
C | G | 1 | a0001c0001t0002g0231 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.156+2740G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115623 | ||||||
| chr12:102115679
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+2684G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115679 | ||||||
| chr12:102115721
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.156+2642T>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115721 | ||||||
| chr12:102115939
|
A | G | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.156+2424T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102115939 | ||||||
| chr12:102116153
|
C | A | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2210G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116153 | ||||||
| chr12:102116206
|
CCT | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | HG02258.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+2155_156+2156d others(4): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116206 | ||||||
| chr12:102116260
|
C | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+2103G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116260 | ||||||
| chr12:102116298
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0080others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+2065T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116298 | ||||||
| chr12:102116430
|
G | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 64 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+1933C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116430 | ||||||
| chr12:102116623
|
A | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 74 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.156+1740T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116623 | ||||||
| chr12:102116786
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+1577G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116786 | ||||||
| chr12:102116806
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+1557G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116806 | ||||||
| chr12:102116897
|
G | A | 2 | a0001c0001t0003g0224a0001c0001t0003g0225 | 2 | NA18612.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.156+1466C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116897 | ||||||
| chr12:102116996
|
C | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 74 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.156+1367G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102116996 | ||||||
| chr12:102117029
|
G | T | 1 | a0001c0001t0003g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.156+1334C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117029 | ||||||
| chr12:102117219
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0003g0197a0001c0001t0003g0198others(1): Show | 6 | NA18942.hp1 NA18955.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+1144G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117219 | ||||||
| chr12:102117360
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0229 | 5 | HG00609.hp1 HG00673.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+1003C>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117360 | ||||||
| chr12:102117373
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+990G>A | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117373 | ||||||
| chr12:102117441
|
G | GA | 99 | a0001c0001t0001g0046a0001c0001t0001g0170a0001c0001t0001g0171others(96): Show | 150 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.156+921dupT | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117441 | ||||||
| chr12:102117453
|
T | A | 2 | a0001c0001t0004g0226a0001c0001t0007g0228 | 2 | HG02723.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156+910A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117453 | ||||||
| chr12:102117459
|
T | A | 1 | a0001c0001t0007g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156+904A>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117459 | ||||||
| chr12:102117508
|
T | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+855A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117508 | ||||||
| chr12:102117694
|
TTTTTATT others(7): Show |
T | 96 | a0001c0001t0001g0227a0001c0001t0001g0271a0001c0001t0001g0272others(93): Show | 147 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.156+655_156+668del others(14): Show |
NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117694 | ||||||
| chr12:102117704
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.156+659C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117704 | ||||||
| chr12:102117717
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0178others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.156+646A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117717 | ||||||
| chr12:102117767
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0182others(11): Show | 18 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+596A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102117767 | ||||||
| chr12:102118160
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.156+203G>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102118160 | ||||||
| chr12:102118354
|
T | C | 1 | a0001c0002t0001g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.156+9A>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 2/9 | chr12 | 102118354 | ||||||
| chr12:102119109
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-65-526C>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119109 | ||||||
| chr12:102119272
|
G | C | 49 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0007others(46): Show | 76 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.-65-689C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119272 | ||||||
| chr12:102119357
|
GT | G | 95 | a0001c0001t0001g0227a0001c0001t0001g0271a0001c0001t0001g0272others(92): Show | 146 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.-66+692delA | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119357 | ||||||
| chr12:102119375
|
A | G | 9 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(6): Show | 9 | HG00323.hp1 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-66+675T>C | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119375 | ||||||
| chr12:102119392
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-66+658T>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119392 | ||||||
| chr12:102119753
|
G | C | 48 | a0001c0001t0001g0229a0001c0001t0002g0002a0001c0001t0002g0007others(45): Show | 75 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.-66+297C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119753 | ||||||
| chr12:102119774
|
C | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 8 | HG00323.hp1 HG01496.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66+276G>T | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119774 | ||||||
| chr12:102119877
|
G | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-66+173C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119877 | ||||||
| chr12:102119908
|
G | C | 1 | a0001c0001t0002g0278 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-66+142C>G | NUP37 | ENSG00000075188.9 | transcript | ENST00000552283.6 | protein_coding | 1/9 | chr12 | 102119908 |