Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 644019 |
|---|---|
| ensemblid | ENSG00000215126.12 |
| hgncid | 31978 |
| symbol | ZNG1F |
| name | Zn regulated GTPase metalloprotein activator 1F |
| refseq_nuc | NM_001085457.2 |
| refseq_prot | NP_001078926.1 |
| ensembl_nuc | ENST00000377391.8 |
| ensembl_prot | ENSP00000366608.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 41131309 |
| end | 41189317 |
| strand | - |
| ver | v1.2 |
| region | chr9:41131309-41189317 |
| region5000 | chr9:41126309-41194317 |
| regionname0 | ZNG1F_chr9_41131309_41189317 |
| regionname5000 | ZNG1F_chr9_41126309_41194317 |
| 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 | 395 | 229 | 62 | 48 | 84 | 5 | 28 | 60 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0002 | 0/0 | 395 | 41 | 6 | 9 | 21 | 1 | 4 | 10 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0003 | 0/0 | 395 | 20 | 0 | 0 | 18 | 0 | 2 | 17 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0004 | 0/0 | 395 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0005 | 0/0 | 395 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0006 | 0/0 | 395 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0007 | 0/0 | 395 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0008 | 0/0 | 395 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| 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 | 0/0 | 1188 | 107 | 13 | 24 | 58 | 5 | 7 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0002 | 0/0 | 1188 | 57 | 27 | 7 | 11 | 0 | 12 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0003 | 0/1 | 1188 | 44 | 4 | 16 | 14 | 0 | 9 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0004 | 0/0 | 1188 | 41 | 6 | 9 | 21 | 1 | 4 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0005 | 0/0 | 1188 | 20 | 0 | 0 | 18 | 0 | 2 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0006 | 1/0 | 1188 | 20 | 18 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0007 | 0/0 | 1188 | 6 | 6 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0008 | 0/0 | 1188 | 5 | 0 | 0 | 5 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0010 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0011 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| c0012 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| 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 | 0/1 | 485 | 282 | 62 | 53 | 127 | 6 | 33 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0002 | 1/0 | 485 | 13 | 11 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0003 | 0/0 | 485 | 3 | 0 | 2 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0004 | 0/0 | 485 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0005 | 0/0 | 485 | 2 | 0 | 1 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0006 | 0/0 | 485 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| t0007 | 0/0 | 485 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0002 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| 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 | 0/0 | 1188 | 107 | 13 | 24 | 58 | 5 | 7 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0002 | 0/0 | 1188 | 57 | 27 | 7 | 11 | 0 | 12 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0003 | 0/1 | 1188 | 44 | 4 | 16 | 14 | 0 | 9 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0006 | 1/0 | 1188 | 20 | 18 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0002c0004 | 0/0 | 1188 | 41 | 6 | 9 | 21 | 1 | 4 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0003c0005 | 0/0 | 1188 | 20 | 0 | 0 | 18 | 0 | 2 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0004c0007 | 0/0 | 1188 | 6 | 6 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0005c0008 | 0/0 | 1188 | 5 | 0 | 0 | 5 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0006c0011 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0007c0012 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0008c0010 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1672 | 106 | 12 | 24 | 58 | 5 | 7 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0001t0006 | 0/0 | 1672 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0002t0001 | 0/0 | 1672 | 57 | 27 | 7 | 11 | 0 | 12 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0003t0001 | 0/1 | 1672 | 43 | 4 | 15 | 14 | 0 | 9 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0003t0004 | 0/0 | 1672 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0006t0001 | 0/0 | 1672 | 6 | 6 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0006t0002 | 1/0 | 1672 | 13 | 11 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0006t0007 | 0/0 | 1672 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0001c0009t0001 | 0/0 | 1672 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0002c0004t0001 | 0/0 | 1672 | 36 | 6 | 6 | 20 | 1 | 3 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0002c0004t0003 | 0/0 | 1672 | 3 | 0 | 2 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0002c0004t0005 | 0/0 | 1672 | 2 | 0 | 1 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0003c0005t0001 | 0/0 | 1672 | 20 | 0 | 0 | 18 | 0 | 2 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0004c0007t0001 | 0/0 | 1672 | 6 | 6 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0005c0008t0001 | 0/0 | 1672 | 5 | 0 | 0 | 5 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0006c0011t0004 | 0/0 | 1672 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0007c0012t0001 | 0/0 | 1672 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| a0008c0010t0001 | 0/0 | 1672 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | copy fasta | chr9 | 41126309 | 41194317 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0003t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0002 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0006t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0001c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0002c0004t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0003c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0004c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0005c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0005c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0005c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0005c0008t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0005c0008t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0006c0011t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0007c0012t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| a0008c0010t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00099 | hp2 | a0002 | c0004 | t0001 | g0185 | EUR | GBR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00408 | hp1 | a0002 | c0004 | t0001 | g0198 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00408 | hp2 | a0002 | c0004 | t0001 | g0195 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00558 | hp2 | a0002 | c0004 | t0001 | g0212 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00597 | hp1 | a0002 | c0004 | t0001 | g0204 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0270 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0233 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | CHS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00735 | hp1 | a0002 | c0004 | t0003 | g0074 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0238 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0258 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01069 | hp2 | a0002 | c0004 | t0001 | g0206 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0253 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0016 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0266 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01106 | hp2 | a0002 | c0004 | t0003 | g0073 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0243 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01175 | hp2 | a0008 | c0010 | t0001 | g0046 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0016 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0264 | AMR | PUR | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01255 | hp1 | a0001 | c0003 | t0004 | g0235 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01496 | hp2 | a0001 | c0006 | t0002 | g0002 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01884 | hp2 | a0001 | c0006 | t0001 | g0027 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01891 | hp2 | a0001 | c0006 | t0002 | g0217 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0265 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0197 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01943 | hp1 | a0002 | c0004 | t0005 | g0200 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0272 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0269 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02027 | hp1 | a0002 | c0004 | t0001 | g0187 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02055 | hp2 | a0001 | c0006 | t0007 | g0024 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02056 | hp2 | a0002 | c0004 | t0005 | g0223 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02080 | hp2 | a0002 | c0004 | t0001 | g0196 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02083 | hp1 | a0003 | c0005 | t0001 | g0039 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0248 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02132 | hp2 | a0002 | c0004 | t0001 | g0231 | EAS | KHV | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0245 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0232 | EAS | CDX | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02165 | hp2 | a0002 | c0004 | t0001 | g0194 | EAS | CDX | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0241 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02293 | hp1 | a0002 | c0004 | t0001 | g0207 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02300 | hp1 | a0002 | c0004 | t0001 | g0199 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02451 | hp1 | a0001 | c0006 | t0002 | g0221 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0268 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0184 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02647 | hp1 | a0001 | c0006 | t0002 | g0220 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0244 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02717 | hp1 | a0002 | c0004 | t0001 | g0192 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02723 | hp1 | a0001 | c0006 | t0002 | g0214 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0025 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02818 | hp2 | a0001 | c0006 | t0002 | g0002 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0208 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0202 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02922 | hp1 | a0001 | c0006 | t0001 | g0023 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0226 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02970 | hp1 | a0004 | c0007 | t0001 | g0278 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02970 | hp2 | a0001 | c0006 | t0002 | g0219 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02976 | hp2 | a0004 | c0007 | t0001 | g0280 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0205 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0236 | AFR | GWD | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03130 | hp2 | a0004 | c0007 | t0001 | g0277 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03139 | hp2 | a0004 | c0007 | t0001 | g0282 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0211 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0209 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03486 | hp1 | a0001 | c0006 | t0002 | g0222 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03490 | hp2 | a0003 | c0005 | t0001 | g0047 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0026 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03579 | hp1 | a0001 | c0006 | t0002 | g0218 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03579 | hp2 | a0004 | c0007 | t0001 | g0281 | AFR | MSL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03654 | hp1 | a0002 | c0004 | t0001 | g0190 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03688 | hp1 | a0002 | c0004 | t0001 | g0189 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0158 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03704 | hp1 | a0003 | c0005 | t0001 | g0038 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0271 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0240 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03834 | hp2 | a0002 | c0004 | t0003 | g0072 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0242 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0237 | SAS | BEB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0210 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | STU | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18522 | hp1 | a0001 | c0006 | t0002 | g0215 | AFR | YRI | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18906 | hp2 | a0004 | c0007 | t0001 | g0279 | AFR | YRI | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18942 | hp1 | a0002 | c0004 | t0001 | g0186 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18944 | hp1 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18949 | hp2 | a0003 | c0005 | t0001 | g0005 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18950 | hp1 | a0002 | c0004 | t0001 | g0225 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18954 | hp2 | a0005 | c0008 | t0001 | g0062 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18956 | hp2 | a0005 | c0008 | t0001 | g0060 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18962 | hp2 | a0005 | c0008 | t0001 | g0067 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18965 | hp1 | a0002 | c0004 | t0001 | g0017 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18967 | hp1 | a0005 | c0008 | t0001 | g0061 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18968 | hp2 | a0003 | c0005 | t0001 | g0005 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18970 | hp2 | a0002 | c0004 | t0001 | g0201 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18979 | hp2 | a0002 | c0004 | t0001 | g0191 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18986 | hp1 | a0003 | c0005 | t0001 | g0048 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18987 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18988 | hp2 | a0005 | c0008 | t0001 | g0064 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18990 | hp1 | a0002 | c0004 | t0001 | g0193 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18993 | hp1 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18998 | hp1 | a0002 | c0004 | t0001 | g0203 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19000 | hp2 | a0003 | c0005 | t0001 | g0042 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19004 | hp1 | a0003 | c0005 | t0001 | g0035 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19012 | hp1 | a0003 | c0005 | t0001 | g0044 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19043 | hp1 | a0006 | c0011 | t0004 | g0234 | AFR | LWK | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19055 | hp1 | a0002 | c0004 | t0001 | g0017 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19055 | hp2 | a0003 | c0005 | t0001 | g0037 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19067 | hp2 | a0002 | c0004 | t0001 | g0224 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19070 | hp1 | a0003 | c0005 | t0001 | g0040 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19074 | hp1 | a0003 | c0005 | t0001 | g0036 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19074 | hp2 | a0001 | c0009 | t0001 | g0022 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19079 | hp2 | a0003 | c0005 | t0001 | g0041 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19081 | hp2 | a0002 | c0004 | t0001 | g0188 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19086 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19089 | hp1 | a0003 | c0005 | t0001 | g0049 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA19090 | hp2 | a0003 | c0005 | t0001 | g0045 | EAS | JPT | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ASW | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | CLM | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02109 | hp2 | a0007 | c0012 | t0001 | g0180 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG02559 | hp2 | a0001 | c0006 | t0002 | g0216 | AFR | ACB | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | USA | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | USA | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA20300 | hp1 | a0001 | c0006 | t0002 | g0213 | AFR | USA | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0239 | REF | REF | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| homoSapiens_grch38 | hp1 | a0001 | c0006 | t0002 | g0002 | REF | REF | ZNG1F_chr9_41126309_41194317 | ZNG1F | chr9 | 41126309 | 41194317 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41131745
|
C | G | 2 | a0003a0008 | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
missense_variant | MODERATE | c.1177G>C | p.Val393Leu | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 1236/1672 | 1177/1188 | 393/395 | chr9 | 41131745 | ||
| chr9:41132242
|
C | T | 1 | a0006 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1067G>A | p.Arg356Gln | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 14/15 | 1126/1672 | 1067/1188 | 356/395 | chr9 | 41132242 | ||
| chr9:41133687
|
T | C | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.872A>G | p.Asn291Ser | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 12/15 | 931/1672 | 872/1188 | 291/395 | chr9 | 41133687 | ||
| chr9:41166805
|
C | T | 1 | a0005 | 5 | NA18954.hp2 NA18956.hp2 NA18962.hp2 others(2): Show |
missense_variant | MODERATE | c.554G>A | p.Gly185Asp | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/15 | 613/1672 | 554/1188 | 185/395 | chr9 | 41166805 | ||
| chr9:41174308
|
C | T | 1 | a0008 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.475G>A | p.Asp159Asn | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/15 | 534/1672 | 475/1188 | 159/395 | chr9 | 41174308 | ||
| chr9:41183604
|
A | G | 2 | a0002a0004 | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
missense_variant | MODERATE | c.298T>C | p.Trp100Arg | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/15 | 357/1672 | 298/1188 | 100/395 | chr9 | 41183604 | ||
| chr9:41189179
|
G | C | 1 | a0004 | 6 | HG02970.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
missense_variant | MODERATE | c.80C>G | p.Thr27Arg | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/15 | 139/1672 | 80/1188 | 27/395 | chr9 | 41189179 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41162341
|
T | C | 2 | a0002c0004a0004c0007 | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
synonymous_variant | LOW | c.699A>G | p.Gln233Gln | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/15 | 758/1672 | 699/1188 | 233/395 | chr9 | 41162341 | ||
| chr9:41165039
|
G | A | 3 | a0001c0002a0005c0008a0007c0012 | 63 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(60): Show |
synonymous_variant | LOW | c.624C>T | p.Val208Val | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/15 | 683/1672 | 624/1188 | 208/395 | chr9 | 41165039 | ||
| chr9:41174321
|
G | A | 7 | a0001c0001a0001c0002a0001c0003others(4): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
synonymous_variant | LOW | c.462C>T | p.Ala154Ala | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/15 | 521/1672 | 462/1188 | 154/395 | chr9 | 41174321 | ||
| chr9:41183587
|
G | A | 2 | a0001c0001a0001c0009 | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/15 | 374/1672 | 315/1188 | 105/395 | chr9 | 41183587 | ||
| chr9:41189187
|
G | T | 1 | a0001c0009 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.72C>A | p.Pro24Pro | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/15 | 131/1672 | 72/1188 | 24/395 | chr9 | 41189187 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41131321
|
C | A | 1 | a0002c0004t0003 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*413G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 413 | chr9 | 41131321 | |||||
| chr9:41131474
|
G | A | 1 | a0002c0004t0005 | 2 | HG01943.hp1 HG02056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*260C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 260 | chr9 | 41131474 | |||||
| chr9:41131521
|
A | G | 2 | a0001c0003t0004a0006c0011t0004 | 2 | HG01255.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*213T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 213 | chr9 | 41131521 | |||||
| chr9:41131546
|
G | A | 17 | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(14): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*188C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 188 | chr9 | 41131546 | |||||
| chr9:41131644
|
G | A | 1 | a0001c0006t0007 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 15/15 | 90 | chr9 | 41131644 | |||||
| chr9:41189269
|
A | G | 1 | a0001c0001t0006 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/15 | 11 | chr9 | 41189269 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:41131864
|
G | A | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1082-24C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 14/14 | chr9 | 41131864 | ||||||
| chr9:41131896
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1082-56A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 14/14 | chr9 | 41131896 | ||||||
| chr9:41131983
|
T | C | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1082-143A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 14/14 | chr9 | 41131983 | ||||||
| chr9:41132373
|
T | C | 1 | a0006c0011t0004g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.952-16A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132373 | ||||||
| chr9:41132470
|
A | T | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.952-113T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132470 | ||||||
| chr9:41132554
|
T | C | 1 | a0002c0004t0001g0194 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.952-197A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132554 | ||||||
| chr9:41132608
|
T | A | 1 | a0002c0004t0001g0194 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.952-251A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132608 | ||||||
| chr9:41132625
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.952-268A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132625 | ||||||
| chr9:41132632
|
G | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.952-275C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132632 | ||||||
| chr9:41132703
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.952-346A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132703 | ||||||
| chr9:41132908
|
C | A | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.952-551G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41132908 | ||||||
| chr9:41133035
|
T | C | 1 | a0001c0002t0001g0276 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.951+470A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133035 | ||||||
| chr9:41133074
|
C | T | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.951+431G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133074 | ||||||
| chr9:41133216
|
G | A | 2 | a0001c0006t0001g0211a0001c0006t0001g0226 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.951+289C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133216 | ||||||
| chr9:41133240
|
T | C | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.951+265A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133240 | ||||||
| chr9:41133262
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.951+243T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133262 | ||||||
| chr9:41133294
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.951+211A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133294 | ||||||
| chr9:41133470
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 153 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.951+35C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 13/14 | chr9 | 41133470 | ||||||
| chr9:41133606
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.886-36A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 12/14 | chr9 | 41133606 | ||||||
| chr9:41133607
|
C | T | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.886-37G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 12/14 | chr9 | 41133607 | ||||||
| chr9:41133639
|
T | C | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.885+35A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 12/14 | chr9 | 41133639 | ||||||
| chr9:41133780
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.817-38C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133780 | ||||||
| chr9:41133787
|
A | T | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-45T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133787 | ||||||
| chr9:41133819
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.817-77C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133819 | ||||||
| chr9:41133874
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.817-132A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133874 | ||||||
| chr9:41133892
|
TG | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.817-151delC | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133892 | ||||||
| chr9:41133909
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.817-167G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133909 | ||||||
| chr9:41133999
|
C | T | 1 | a0001c0006t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.817-257G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41133999 | ||||||
| chr9:41134098
|
G | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.817-356C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134098 | ||||||
| chr9:41134102
|
C | A | 11 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0063others(8): Show | 11 | HG01496.hp1 HG02040.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-360G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134102 | ||||||
| chr9:41134205
|
C | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.817-463G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134205 | ||||||
| chr9:41134216
|
G | A | 2 | a0004c0007t0001g0277a0004c0007t0001g0278 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.817-474C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134216 | ||||||
| chr9:41134221
|
C | T | 2 | a0004c0007t0001g0277a0004c0007t0001g0278 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.817-479G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134221 | ||||||
| chr9:41134343
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.817-601A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134343 | ||||||
| chr9:41134349
|
G | C | 12 | a0001c0003t0001g0245a0001c0003t0001g0247a0001c0003t0001g0250others(9): Show | 12 | HG00544.hp1 HG00673.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-607C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134349 | ||||||
| chr9:41134445
|
A | G | 19 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(16): Show | 19 | HG00423.hp2 HG01496.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-703T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134445 | ||||||
| chr9:41134492
|
C | CT | 7 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0107others(4): Show | 9 | HG00639.hp1 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-751dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134492 | ||||||
| chr9:41134688
|
G | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.817-946C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134688 | ||||||
| chr9:41134961
|
A | C | 1 | a0001c0003t0001g0019 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.817-1219T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134961 | ||||||
| chr9:41134963
|
C | T | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-1221G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134963 | ||||||
| chr9:41134989
|
C | T | 1 | a0007c0012t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.817-1247G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41134989 | ||||||
| chr9:41135019
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-1277T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135019 | ||||||
| chr9:41135023
|
T | C | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.817-1281A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135023 | ||||||
| chr9:41135074
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.817-1332G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135074 | ||||||
| chr9:41135152
|
G | T | 1 | a0001c0002t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.817-1410C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135152 | ||||||
| chr9:41135306
|
G | A | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.817-1564C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135306 | ||||||
| chr9:41135410
|
G | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.817-1668C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135410 | ||||||
| chr9:41135455
|
C | A | 1 | a0001c0002t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.817-1713G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135455 | ||||||
| chr9:41135460
|
C | T | 3 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0007g0024 | 3 | HG02055.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.817-1718G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135460 | ||||||
| chr9:41135478
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-1736G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135478 | ||||||
| chr9:41135480
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.817-1738C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135480 | ||||||
| chr9:41135616
|
CAT | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.817-1876_817-1875d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135616 | ||||||
| chr9:41135806
|
C | G | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.817-2064G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135806 | ||||||
| chr9:41135981
|
A | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-2239T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41135981 | ||||||
| chr9:41136047
|
C | T | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.817-2305G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136047 | ||||||
| chr9:41136048
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-2306A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136048 | ||||||
| chr9:41136082
|
G | A | 7 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-2340C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136082 | ||||||
| chr9:41136085
|
G | A | 1 | a0003c0005t0001g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-2343C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136085 | ||||||
| chr9:41136165
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0007c0012t0001g0180 | 3 | HG02109.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.817-2423G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136165 | ||||||
| chr9:41136214
|
G | A | 1 | a0001c0003t0001g0241 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.817-2472C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136214 | ||||||
| chr9:41136218
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.817-2476G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136218 | ||||||
| chr9:41136249
|
A | T | 1 | a0002c0004t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.817-2507T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136249 | ||||||
| chr9:41136255
|
T | C | 1 | a0003c0005t0001g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-2513A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136255 | ||||||
| chr9:41136316
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-2574G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136316 | ||||||
| chr9:41136477
|
T | TTA | 220 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 238 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.817-2736_817-2735i others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136477 | ||||||
| chr9:41136640
|
A | AT | 44 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(41): Show | 46 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.817-2899dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136640 | ||||||
| chr9:41136683
|
G | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-2941C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136683 | ||||||
| chr9:41136748
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.817-3006C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136748 | ||||||
| chr9:41136856
|
T | A | 1 | a0002c0004t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.817-3114A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136856 | ||||||
| chr9:41136973
|
A | G | 10 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(7): Show | 10 | HG01928.hp1 HG02074.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-3231T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41136973 | ||||||
| chr9:41137009
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0094others(7): Show | 12 | HG00733.hp2 HG01070.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-3267G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137009 | ||||||
| chr9:41137035
|
G | A | 1 | a0001c0001t0001g0013 | 2 | NA18939.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.817-3293C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137035 | ||||||
| chr9:41137080
|
T | C | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.817-3338A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137080 | ||||||
| chr9:41137106
|
T | G | 1 | a0001c0002t0001g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.817-3364A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137106 | ||||||
| chr9:41137184
|
G | T | 1 | a0001c0002t0001g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.817-3442C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137184 | ||||||
| chr9:41137186
|
C | T | 1 | a0006c0011t0004g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.817-3444G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137186 | ||||||
| chr9:41137259
|
ATTCCATG others(43): Show |
A | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-3567_817-3518d others(52): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137259 | ||||||
| chr9:41137282
|
G | A | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-3540C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137282 | ||||||
| chr9:41137437
|
G | T | 4 | a0001c0003t0001g0249a0001c0003t0001g0253a0001c0003t0001g0258others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-3695C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137437 | ||||||
| chr9:41137448
|
GGTT | G | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.817-3709_817-3707d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137448 | ||||||
| chr9:41137774
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-4032T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137774 | ||||||
| chr9:41137829
|
C | T | 19 | a0001c0001t0001g0112a0003c0005t0001g0003a0003c0005t0001g0004others(16): Show | 22 | HG00735.hp2 HG01175.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.817-4087G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41137829 | ||||||
| chr9:41138044
|
G | GT | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.817-4303dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138044 | ||||||
| chr9:41138045
|
T | G | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4303A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138045 | ||||||
| chr9:41138069
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4327A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138069 | ||||||
| chr9:41138126
|
T | A | 3 | a0002c0004t0001g0189a0002c0004t0001g0190a0002c0004t0001g0210 | 3 | HG03654.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.817-4384A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138126 | ||||||
| chr9:41138131
|
C | A | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4389G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138131 | ||||||
| chr9:41138132
|
G | A | 1 | a0002c0004t0001g0016 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-4390C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138132 | ||||||
| chr9:41138222
|
T | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-4480A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138222 | ||||||
| chr9:41138227
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4485G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138227 | ||||||
| chr9:41138232
|
A | G | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.817-4490T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138232 | ||||||
| chr9:41138291
|
G | A | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0007c0012t0001g0180 | 3 | HG02109.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.817-4549C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138291 | ||||||
| chr9:41138331
|
G | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4589C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138331 | ||||||
| chr9:41138377
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4635G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138377 | ||||||
| chr9:41138426
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4684A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138426 | ||||||
| chr9:41138457
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4715A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138457 | ||||||
| chr9:41138468
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4726G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138468 | ||||||
| chr9:41138700
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-4958A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138700 | ||||||
| chr9:41138711
|
A | G | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-4969T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138711 | ||||||
| chr9:41138759
|
C | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-5017G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138759 | ||||||
| chr9:41138765
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-5023G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138765 | ||||||
| chr9:41138891
|
T | A | 2 | a0001c0002t0001g0068a0001c0002t0001g0230 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.817-5149A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138891 | ||||||
| chr9:41138893
|
T | A | 58 | a0001c0001t0001g0108a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.817-5151A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41138893 | ||||||
| chr9:41139031
|
T | G | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-5289A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139031 | ||||||
| chr9:41139074
|
G | A | 1 | a0001c0003t0001g0255 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.817-5332C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139074 | ||||||
| chr9:41139083
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.817-5341C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139083 | ||||||
| chr9:41139154
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 217 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.817-5412T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139154 | ||||||
| chr9:41139172
|
T | C | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-5430A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139172 | ||||||
| chr9:41139239
|
A | C | 1 | a0001c0002t0001g0273 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.817-5497T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139239 | ||||||
| chr9:41139269
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-5527C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139269 | ||||||
| chr9:41139285
|
G | C | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-5543C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139285 | ||||||
| chr9:41139286
|
C | T | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-5544G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139286 | ||||||
| chr9:41139287
|
T | G | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-5545A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139287 | ||||||
| chr9:41139316
|
G | C | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.817-5574C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139316 | ||||||
| chr9:41139356
|
C | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-5614G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139356 | ||||||
| chr9:41139428
|
A | G | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.817-5686T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139428 | ||||||
| chr9:41139481
|
A | G | 1 | a0003c0005t0001g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-5739T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139481 | ||||||
| chr9:41139588
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0142a0001c0006t0001g0226 | 3 | HG02965.hp1 NA18984.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.816+5693G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139588 | ||||||
| chr9:41139589
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.816+5692C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139589 | ||||||
| chr9:41139622
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.816+5659G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139622 | ||||||
| chr9:41139676
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 109 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.816+5605C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139676 | ||||||
| chr9:41139783
|
A | T | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.816+5498T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139783 | ||||||
| chr9:41139806
|
ATAC | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0118others(2): Show | 5 | HG01257.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+5472_816+5474d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139806 | ||||||
| chr9:41139885
|
T | A | 4 | a0002c0004t0001g0193a0002c0004t0001g0194a0002c0004t0001g0195others(1): Show | 4 | HG00408.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+5396A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139885 | ||||||
| chr9:41139966
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.816+5315G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41139966 | ||||||
| chr9:41140052
|
T | G | 2 | a0001c0002t0001g0230a0001c0002t0001g0273 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+5229A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140052 | ||||||
| chr9:41140075
|
A | G | 1 | a0001c0002t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.816+5206T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140075 | ||||||
| chr9:41140101
|
A | G | 3 | a0001c0002t0001g0058a0001c0002t0001g0065a0001c0002t0001g0066 | 3 | HG01496.hp1 HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.816+5180T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140101 | ||||||
| chr9:41140150
|
GATAC | G | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+5127_816+5130d others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140150 | ||||||
| chr9:41140208
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+5073A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140208 | ||||||
| chr9:41140267
|
G | A | 1 | a0002c0004t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.816+5014C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140267 | ||||||
| chr9:41140298
|
A | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+4983T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140298 | ||||||
| chr9:41140309
|
T | A | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.816+4972A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140309 | ||||||
| chr9:41140324
|
C | G | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+4957G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140324 | ||||||
| chr9:41140325
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+4956C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140325 | ||||||
| chr9:41140341
|
G | GGTAA | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.816+4939_816+4940i others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140341 | ||||||
| chr9:41140375
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.816+4906T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140375 | ||||||
| chr9:41140528
|
T | A | 1 | a0002c0004t0001g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.816+4753A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140528 | ||||||
| chr9:41140801
|
C | G | 1 | a0003c0005t0001g0036 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.816+4480G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140801 | ||||||
| chr9:41140851
|
G | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.816+4430C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140851 | ||||||
| chr9:41140925
|
C | G | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+4356G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140925 | ||||||
| chr9:41140965
|
C | A | 1 | a0001c0002t0001g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.816+4316G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140965 | ||||||
| chr9:41140990
|
AG | A | 32 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(29): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.816+4290delC | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140990 | ||||||
| chr9:41140992
|
C | T | 32 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(29): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.816+4289G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41140992 | ||||||
| chr9:41141115
|
G | T | 3 | a0004c0007t0001g0277a0004c0007t0001g0278a0004c0007t0001g0282 | 3 | HG02970.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+4166C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141115 | ||||||
| chr9:41141184
|
C | T | 1 | a0001c0003t0004g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.816+4097G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141184 | ||||||
| chr9:41141196
|
C | A | 1 | a0001c0002t0001g0276 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.816+4085G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141196 | ||||||
| chr9:41141635
|
C | A | 52 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(49): Show | 54 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.816+3646G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141635 | ||||||
| chr9:41141730
|
A | C | 1 | a0001c0006t0002g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.816+3551T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141730 | ||||||
| chr9:41141815
|
G | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.816+3466C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141815 | ||||||
| chr9:41141944
|
C | T | 1 | a0003c0005t0001g0049 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.816+3337G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141944 | ||||||
| chr9:41141945
|
T | C | 1 | a0003c0005t0001g0049 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.816+3336A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41141945 | ||||||
| chr9:41142073
|
G | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+3208C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142073 | ||||||
| chr9:41142246
|
C | T | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3035G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142246 | ||||||
| chr9:41142430
|
G | C | 4 | a0001c0003t0001g0249a0001c0003t0001g0253a0001c0003t0001g0258others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+2851C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142430 | ||||||
| chr9:41142474
|
T | C | 1 | a0002c0004t0001g0188 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.816+2807A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142474 | ||||||
| chr9:41142555
|
G | A | 1 | a0001c0002t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.816+2726C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142555 | ||||||
| chr9:41142595
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.816+2686C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142595 | ||||||
| chr9:41142641
|
T | TA | 9 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0006t0001g0026others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.816+2639dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAA | 9 | a0001c0002t0001g0028a0001c0002t0001g0031a0001c0002t0001g0032others(6): Show | 9 | HG01884.hp2 HG02602.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+2638_816+2639d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAA | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0030others(16): Show | 21 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.816+2637_816+2639d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAAA | 28 | a0001c0002t0001g0029a0001c0002t0001g0055a0001c0002t0001g0056others(25): Show | 29 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.816+2636_816+2639d others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAAAA | 22 | a0001c0002t0001g0054a0001c0002t0001g0057a0001c0002t0001g0065others(19): Show | 23 | HG00423.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.816+2635_816+2639d others(7): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAAAAA | 7 | a0001c0002t0001g0053a0001c0002t0001g0058a0001c0002t0001g0069others(4): Show | 7 | HG01106.hp2 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+2634_816+2639d others(8): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAAAAAA | 6 | a0001c0002t0001g0052a0001c0002t0001g0063a0002c0004t0001g0225others(3): Show | 6 | HG02040.hp1 HG03453.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2633_816+2639d others(9): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
T | TAAAAAAA others(3): Show |
1 | a0002c0004t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.816+2630_816+2639d others(12): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(2): Show |
T | 13 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(10): Show | 16 | HG02083.hp1 HG03490.hp2 HG03704.hp1 others(13): Show |
intron_variant | MODIFIER | c.816+2631_816+2639d others(11): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(3): Show |
T | 7 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | NA18969.hp2 NA18986.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+2630_816+2639d others(12): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(4): Show |
T | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(10): Show | 16 | HG00423.hp1 HG00733.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.816+2629_816+2639d others(13): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(5): Show |
T | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 93 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+2628_816+2639d others(14): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(6): Show |
T | 36 | a0001c0001t0001g0083a0001c0003t0001g0018a0001c0003t0001g0019others(33): Show | 39 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.816+2627_816+2639d others(15): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142641
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0002t0001g0164a0001c0003t0001g0255 | 2 | HG02056.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.816+2626_816+2639d others(16): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142641 | ||||||
| chr9:41142743
|
G | C | 1 | a0001c0003t0001g0270 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.816+2538C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142743 | ||||||
| chr9:41142840
|
T | G | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.816+2441A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142840 | ||||||
| chr9:41142850
|
C | A | 40 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(37): Show | 43 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.816+2431G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142850 | ||||||
| chr9:41142912
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.816+2369T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41142912 | ||||||
| chr9:41143023
|
A | G | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.816+2258T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143023 | ||||||
| chr9:41143150
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+2131G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143150 | ||||||
| chr9:41143151
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+2130G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143151 | ||||||
| chr9:41143262
|
A | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+2019T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143262 | ||||||
| chr9:41143431
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.816+1850G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143431 | ||||||
| chr9:41143585
|
G | T | 1 | a0001c0002t0001g0054 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.816+1696C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143585 | ||||||
| chr9:41143691
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.816+1590T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143691 | ||||||
| chr9:41143722
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+1559A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143722 | ||||||
| chr9:41143774
|
A | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.816+1507T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143774 | ||||||
| chr9:41143994
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.816+1287T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41143994 | ||||||
| chr9:41144002
|
T | A | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.816+1279A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144002 | ||||||
| chr9:41144011
|
A | T | 2 | a0001c0002t0001g0273a0001c0006t0001g0027 | 2 | HG01175.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.816+1270T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144011 | ||||||
| chr9:41144044
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.816+1237A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144044 | ||||||
| chr9:41144052
|
G | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | NA18939.hp2 NA18970.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1229C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144052 | ||||||
| chr9:41144064
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.816+1217A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144064 | ||||||
| chr9:41144158
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.816+1123C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144158 | ||||||
| chr9:41144308
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 237 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.816+973A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144308 | ||||||
| chr9:41144387
|
GT | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 92 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.816+893delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144387 | ||||||
| chr9:41144387
|
GTT | G | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.816+892_816+893del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144387 | ||||||
| chr9:41144565
|
GC | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.816+715delG | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144565 | ||||||
| chr9:41144685
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.816+596A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144685 | ||||||
| chr9:41144746
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.816+535G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144746 | ||||||
| chr9:41144881
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.816+400G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144881 | ||||||
| chr9:41144905
|
C | T | 1 | a0001c0003t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.816+376G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144905 | ||||||
| chr9:41144916
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.816+365G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41144916 | ||||||
| chr9:41145039
|
TAG | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 7 | NA18939.hp2 NA18970.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+240_816+241del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41145039 | ||||||
| chr9:41145092
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+189T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41145092 | ||||||
| chr9:41145206
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.816+75T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 11/14 | chr9 | 41145206 | ||||||
| chr9:41145389
|
C | T | 2 | a0001c0006t0001g0211a0001c0006t0001g0226 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.765-57G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145389 | ||||||
| chr9:41145537
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.765-205G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145537 | ||||||
| chr9:41145646
|
T | C | 3 | a0002c0004t0001g0192a0002c0004t0001g0205a0002c0004t0001g0208 | 3 | HG02717.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.765-314A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145646 | ||||||
| chr9:41145688
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.765-356A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145688 | ||||||
| chr9:41145746
|
G | T | 32 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(29): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.765-414C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145746 | ||||||
| chr9:41145857
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-525T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145857 | ||||||
| chr9:41145863
|
A | C | 1 | a0002c0004t0001g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.765-531T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145863 | ||||||
| chr9:41145979
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.765-647C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41145979 | ||||||
| chr9:41146000
|
G | T | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.765-668C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146000 | ||||||
| chr9:41146027
|
AG | A | 3 | a0001c0003t0001g0018a0001c0003t0001g0236a0003c0005t0001g0047 | 4 | HG02280.hp2 HG03041.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-696delC | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146027 | ||||||
| chr9:41146040
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.765-708C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146040 | ||||||
| chr9:41146117
|
T | G | 1 | a0001c0002t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.765-785A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146117 | ||||||
| chr9:41146125
|
A | G | 5 | a0001c0001t0001g0154a0001c0002t0001g0164a0001c0003t0001g0245others(2): Show | 5 | HG00099.hp2 HG02148.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-793T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146125 | ||||||
| chr9:41146153
|
G | A | 3 | a0001c0001t0001g0123a0001c0003t0004g0235a0002c0004t0001g0198 | 3 | HG00408.hp1 HG01255.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.765-821C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146153 | ||||||
| chr9:41146216
|
T | C | 5 | a0001c0001t0001g0011a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 6 | HG01123.hp1 HG01515.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.765-884A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146216 | ||||||
| chr9:41146269
|
A | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.765-937T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146269 | ||||||
| chr9:41146282
|
T | G | 1 | a0001c0002t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.765-950A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146282 | ||||||
| chr9:41146334
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.765-1002A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146334 | ||||||
| chr9:41146345
|
T | TC | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.765-1014dupG | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146345 | ||||||
| chr9:41146348
|
T | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.765-1016A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146348 | ||||||
| chr9:41146398
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.765-1066G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146398 | ||||||
| chr9:41146403
|
C | CA | 18 | a0001c0002t0001g0158a0001c0002t0001g0175a0001c0002t0001g0176others(15): Show | 19 | HG00639.hp2 HG01099.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.765-1072dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146403 | ||||||
| chr9:41146403
|
C | CAA | 10 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273others(7): Show | 11 | HG01175.hp1 HG01243.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.765-1073_765-1072d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146403 | ||||||
| chr9:41146403
|
CA | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.765-1072delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146403 | ||||||
| chr9:41146403
|
CAA | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0082others(4): Show | 7 | HG01255.hp2 NA18944.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.765-1073_765-1072d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146403 | ||||||
| chr9:41146482
|
AT | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.765-1151delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146482 | ||||||
| chr9:41146636
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.765-1304C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146636 | ||||||
| chr9:41146640
|
G | A | 4 | a0001c0003t0001g0250a0001c0003t0001g0254a0001c0003t0001g0260others(1): Show | 4 | HG00544.hp1 HG02027.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-1308C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146640 | ||||||
| chr9:41146643
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.765-1311A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146643 | ||||||
| chr9:41146827
|
A | G | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.765-1495T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146827 | ||||||
| chr9:41146904
|
C | G | 4 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161others(1): Show | 4 | NA18980.hp2 NA18990.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-1572G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146904 | ||||||
| chr9:41146986
|
T | C | 3 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0056 | 3 | HG00423.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.765-1654A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41146986 | ||||||
| chr9:41147151
|
T | C | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.765-1819A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147151 | ||||||
| chr9:41147228
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | NA18939.hp2 NA18970.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.765-1896G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147228 | ||||||
| chr9:41147239
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.765-1907T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147239 | ||||||
| chr9:41147284
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.765-1952A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147284 | ||||||
| chr9:41147304
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765-1972A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147304 | ||||||
| chr9:41147316
|
C | T | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.765-1984G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147316 | ||||||
| chr9:41147366
|
A | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.765-2034T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147366 | ||||||
| chr9:41147412
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.765-2080C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147412 | ||||||
| chr9:41147414
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.765-2082G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147414 | ||||||
| chr9:41147421
|
C | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.765-2089G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147421 | ||||||
| chr9:41147448
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-2116G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147448 | ||||||
| chr9:41147472
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.765-2140T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147472 | ||||||
| chr9:41147535
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.765-2203A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147535 | ||||||
| chr9:41147565
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.765-2233G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147565 | ||||||
| chr9:41147608
|
G | A | 1 | a0002c0004t0001g0204 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.765-2276C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147608 | ||||||
| chr9:41147617
|
G | A | 16 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(13): Show | 19 | HG01175.hp2 HG02083.hp1 NA18944.hp1 others(16): Show |
intron_variant | MODIFIER | c.765-2285C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147617 | ||||||
| chr9:41147618
|
A | T | 16 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(13): Show | 19 | HG01175.hp2 HG02083.hp1 NA18944.hp1 others(16): Show |
intron_variant | MODIFIER | c.765-2286T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147618 | ||||||
| chr9:41147651
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.765-2319G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147651 | ||||||
| chr9:41147679
|
G | GAA | 39 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(36): Show | 42 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.765-2349_765-2348d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147679 | ||||||
| chr9:41147680
|
A | G | 52 | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(49): Show | 53 | HG00423.hp2 HG00733.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.765-2348T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147680 | ||||||
| chr9:41147719
|
G | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.765-2387C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147719 | ||||||
| chr9:41147727
|
G | T | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.765-2395C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147727 | ||||||
| chr9:41147782
|
G | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.765-2450C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147782 | ||||||
| chr9:41147827
|
G | A | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.765-2495C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147827 | ||||||
| chr9:41147860
|
G | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.765-2528C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147860 | ||||||
| chr9:41147918
|
G | A | 1 | a0003c0005t0001g0041 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.765-2586C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147918 | ||||||
| chr9:41147993
|
C | T | 2 | a0001c0002t0001g0070a0001c0002t0001g0273 | 2 | HG01175.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.765-2661G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41147993 | ||||||
| chr9:41148092
|
G | A | 1 | a0004c0007t0001g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.765-2760C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148092 | ||||||
| chr9:41148106
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.765-2774A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148106 | ||||||
| chr9:41148446
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.765-3114A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148446 | ||||||
| chr9:41148574
|
T | C | 1 | a0002c0004t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.765-3242A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148574 | ||||||
| chr9:41148707
|
T | TA | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765-3376_765-3375i others(3): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148707 | ||||||
| chr9:41148708
|
C | A | 55 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(52): Show | 57 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.765-3376G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148708 | ||||||
| chr9:41148708
|
C | CT | 87 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.765-3377dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148708 | ||||||
| chr9:41148708
|
C | CTT | 14 | a0001c0001t0001g0080a0001c0003t0001g0245a0001c0003t0001g0247others(11): Show | 14 | HG00544.hp1 HG00673.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.765-3378_765-3377d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148708 | ||||||
| chr9:41148708
|
C | CTTT | 30 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(27): Show | 33 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.765-3379_765-3377d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148708 | ||||||
| chr9:41148708
|
C | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765-3376G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148708 | ||||||
| chr9:41148755
|
TAAAGTA | T | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-3429_765-3424d others(8): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41148755 | ||||||
| chr9:41149293
|
C | A | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.765-3961G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149293 | ||||||
| chr9:41149365
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.765-4033A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149365 | ||||||
| chr9:41149367
|
T | C | 1 | a0001c0003t0004g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765-4035A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149367 | ||||||
| chr9:41149403
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.765-4071G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149403 | ||||||
| chr9:41149417
|
G | A | 1 | a0001c0003t0001g0255 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.765-4085C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149417 | ||||||
| chr9:41149451
|
G | C | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.765-4119C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149451 | ||||||
| chr9:41149807
|
A | C | 2 | a0002c0004t0001g0231a0002c0004t0001g0232 | 2 | HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.765-4475T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149807 | ||||||
| chr9:41149871
|
A | G | 1 | a0006c0011t0004g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.765-4539T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149871 | ||||||
| chr9:41149872
|
G | C | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.765-4540C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149872 | ||||||
| chr9:41149934
|
T | C | 54 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.765-4602A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149934 | ||||||
| chr9:41149959
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.765-4627C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149959 | ||||||
| chr9:41149996
|
G | A | 1 | a0001c0003t0001g0251 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.765-4664C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41149996 | ||||||
| chr9:41150021
|
C | T | 3 | a0001c0002t0001g0015a0001c0002t0001g0176a0001c0002t0001g0177 | 4 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-4689G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150021 | ||||||
| chr9:41150022
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.765-4690C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150022 | ||||||
| chr9:41150042
|
A | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 237 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.765-4710T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150042 | ||||||
| chr9:41150062
|
G | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0151 | 2 | HG02165.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.765-4730C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150062 | ||||||
| chr9:41150079
|
T | G | 1 | a0001c0009t0001g0022 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.765-4747A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150079 | ||||||
| chr9:41150086
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.765-4754C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150086 | ||||||
| chr9:41150091
|
G | C | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.765-4759C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150091 | ||||||
| chr9:41150111
|
G | C | 1 | a0001c0009t0001g0022 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.765-4779C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150111 | ||||||
| chr9:41150216
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.765-4884C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150216 | ||||||
| chr9:41150300
|
C | T | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.765-4968G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150300 | ||||||
| chr9:41150323
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.765-4991G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150323 | ||||||
| chr9:41150330
|
G | T | 1 | a0002c0004t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.765-4998C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150330 | ||||||
| chr9:41150334
|
T | C | 2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG02132.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.765-5002A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150334 | ||||||
| chr9:41150378
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.765-5046G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150378 | ||||||
| chr9:41150556
|
C | T | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.765-5224G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150556 | ||||||
| chr9:41150565
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.765-5233G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150565 | ||||||
| chr9:41150631
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0002t0001g0070others(2): Show | 5 | HG01175.hp1 HG02615.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-5299G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150631 | ||||||
| chr9:41150664
|
C | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765-5332G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150664 | ||||||
| chr9:41150725
|
C | A | 54 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.765-5393G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150725 | ||||||
| chr9:41150759
|
G | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0144 | 3 | HG01074.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.765-5427C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150759 | ||||||
| chr9:41150963
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+5420G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150963 | ||||||
| chr9:41150977
|
A | G | 3 | a0002c0004t0001g0192a0002c0004t0001g0205a0002c0004t0001g0208 | 3 | HG02717.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.764+5406T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150977 | ||||||
| chr9:41150997
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.764+5386G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41150997 | ||||||
| chr9:41151059
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.764+5324G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151059 | ||||||
| chr9:41151316
|
A | G | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.764+5067T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151316 | ||||||
| chr9:41151407
|
ACCAAGTT others(13): Show |
A | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.764+4956_764+4975d others(22): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151407 | ||||||
| chr9:41151457
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.764+4926A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151457 | ||||||
| chr9:41151476
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+4907T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151476 | ||||||
| chr9:41151481
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.764+4902C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151481 | ||||||
| chr9:41151510
|
G | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.764+4873C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151510 | ||||||
| chr9:41151664
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.764+4719A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151664 | ||||||
| chr9:41151700
|
C | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+4683G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151700 | ||||||
| chr9:41151714
|
A | G | 2 | a0001c0002t0001g0058a0001c0002t0001g0066 | 2 | HG01496.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.764+4669T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151714 | ||||||
| chr9:41151800
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 152 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.764+4583G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151800 | ||||||
| chr9:41151804
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.764+4579C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151804 | ||||||
| chr9:41151853
|
G | A | 1 | a0002c0004t0001g0016 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.764+4530C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151853 | ||||||
| chr9:41151859
|
C | G | 1 | a0001c0001t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.764+4524G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151859 | ||||||
| chr9:41151947
|
C | T | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.764+4436G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151947 | ||||||
| chr9:41151950
|
G | A | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.764+4433C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41151950 | ||||||
| chr9:41152031
|
G | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.764+4352C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152031 | ||||||
| chr9:41152089
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+4294C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152089 | ||||||
| chr9:41152107
|
A | T | 1 | a0003c0005t0001g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.764+4276T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152107 | ||||||
| chr9:41152113
|
C | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.764+4270G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152113 | ||||||
| chr9:41152115
|
T | G | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.764+4268A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152115 | ||||||
| chr9:41152132
|
G | C | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.764+4251C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152132 | ||||||
| chr9:41152144
|
G | A | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.764+4239C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152144 | ||||||
| chr9:41152226
|
C | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.764+4157G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152226 | ||||||
| chr9:41152339
|
C | A | 56 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(53): Show | 58 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.764+4044G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152339 | ||||||
| chr9:41152367
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01123.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.764+4016G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152367 | ||||||
| chr9:41152403
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.764+3980C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152403 | ||||||
| chr9:41152525
|
C | T | 1 | a0006c0011t0004g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.764+3858G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152525 | ||||||
| chr9:41152574
|
T | C | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.764+3809A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152574 | ||||||
| chr9:41152595
|
C | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0111a0001c0001t0001g0124 | 3 | HG01070.hp2 HG01257.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.764+3788G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152595 | ||||||
| chr9:41152748
|
G | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.764+3635C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152748 | ||||||
| chr9:41152766
|
G | A | 2 | a0001c0002t0001g0058a0001c0002t0001g0230 | 2 | HG02109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.764+3617C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152766 | ||||||
| chr9:41152844
|
T | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.764+3539A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152844 | ||||||
| chr9:41152877
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.764+3506A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41152877 | ||||||
| chr9:41153019
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 211 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.764+3364T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153019 | ||||||
| chr9:41153098
|
A | C | 1 | a0001c0002t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.764+3285T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153098 | ||||||
| chr9:41153099
|
C | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.764+3284G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153099 | ||||||
| chr9:41153122
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.764+3261T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153122 | ||||||
| chr9:41153126
|
A | G | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.764+3257T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153126 | ||||||
| chr9:41153127
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.764+3256C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153127 | ||||||
| chr9:41153128
|
A | G | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.764+3255T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153128 | ||||||
| chr9:41153166
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+3217C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153166 | ||||||
| chr9:41153218
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.764+3165T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153218 | ||||||
| chr9:41153232
|
C | T | 1 | a0002c0004t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.764+3151G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153232 | ||||||
| chr9:41153283
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0145 | 2 | NA18747.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.764+3100G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153283 | ||||||
| chr9:41153407
|
C | T | 1 | a0001c0003t0004g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.764+2976G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153407 | ||||||
| chr9:41153584
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+2799G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153584 | ||||||
| chr9:41153620
|
C | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+2763G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153620 | ||||||
| chr9:41153682
|
C | T | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.764+2701G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153682 | ||||||
| chr9:41153689
|
C | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.764+2694G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153689 | ||||||
| chr9:41153754
|
A | G | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+2629T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153754 | ||||||
| chr9:41153848
|
G | A | 38 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0237others(35): Show | 40 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.764+2535C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153848 | ||||||
| chr9:41153901
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.764+2482A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41153901 | ||||||
| chr9:41154056
|
G | A | 2 | a0001c0002t0001g0059a0001c0002t0001g0063 | 2 | HG02040.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.764+2327C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154056 | ||||||
| chr9:41154079
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0002t0001g0070others(2): Show | 5 | HG01175.hp1 HG02615.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.764+2304G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154079 | ||||||
| chr9:41154099
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.764+2284T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154099 | ||||||
| chr9:41154109
|
C | T | 6 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0070others(3): Show | 6 | HG01175.hp1 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.764+2274G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154109 | ||||||
| chr9:41154294
|
C | G | 33 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(30): Show | 35 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.764+2089G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154294 | ||||||
| chr9:41154315
|
T | A | 2 | a0001c0006t0001g0211a0001c0006t0001g0226 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.764+2068A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154315 | ||||||
| chr9:41154400
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.764+1983T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154400 | ||||||
| chr9:41154405
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1978T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154405 | ||||||
| chr9:41154410
|
C | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1973G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154410 | ||||||
| chr9:41154420
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0094others(7): Show | 12 | HG00733.hp2 HG01070.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.764+1963G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154420 | ||||||
| chr9:41154428
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1955G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154428 | ||||||
| chr9:41154542
|
G | A | 1 | a0007c0012t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.764+1841C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154542 | ||||||
| chr9:41154547
|
G | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+1836C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154547 | ||||||
| chr9:41154596
|
T | A | 1 | a0001c0002t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.764+1787A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154596 | ||||||
| chr9:41154659
|
A | G | 1 | a0002c0004t0001g0206 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.764+1724T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154659 | ||||||
| chr9:41154702
|
A | G | 1 | a0001c0006t0002g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.764+1681T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154702 | ||||||
| chr9:41154790
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.764+1593G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154790 | ||||||
| chr9:41154823
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.764+1560G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154823 | ||||||
| chr9:41154954
|
CAT | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.764+1427_764+1428d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154954 | ||||||
| chr9:41154980
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0139 | 4 | NA18956.hp1 NA18975.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1403A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154980 | ||||||
| chr9:41154989
|
C | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0139 | 4 | NA18956.hp1 NA18975.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1394G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41154989 | ||||||
| chr9:41155034
|
C | A | 1 | a0001c0002t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.764+1349G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155034 | ||||||
| chr9:41155056
|
A | G | 1 | a0003c0005t0001g0047 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.764+1327T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155056 | ||||||
| chr9:41155086
|
A | C | 2 | a0001c0001t0001g0101a0001c0002t0001g0182 | 2 | HG02622.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.764+1297T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155086 | ||||||
| chr9:41155093
|
G | A | 1 | a0001c0003t0001g0270 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.764+1290C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155093 | ||||||
| chr9:41155093
|
G | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0082others(1): Show | 4 | NA18984.hp2 NA18986.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+1290C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155093 | ||||||
| chr9:41155094
|
C | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+1289G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155094 | ||||||
| chr9:41155153
|
T | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.764+1230A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155153 | ||||||
| chr9:41155191
|
G | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0034 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.764+1192C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155191 | ||||||
| chr9:41155200
|
G | A | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.764+1183C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155200 | ||||||
| chr9:41155233
|
C | A | 1 | a0001c0006t0002g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.764+1150G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155233 | ||||||
| chr9:41155234
|
A | G | 1 | a0001c0006t0002g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.764+1149T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155234 | ||||||
| chr9:41155272
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1111G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155272 | ||||||
| chr9:41155633
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.764+750A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155633 | ||||||
| chr9:41155695
|
A | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+688T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155695 | ||||||
| chr9:41155695
|
A | T | 3 | a0004c0007t0001g0279a0004c0007t0001g0280a0004c0007t0001g0281 | 3 | HG02976.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.764+688T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155695 | ||||||
| chr9:41155698
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+685A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155698 | ||||||
| chr9:41155753
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.764+630A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155753 | ||||||
| chr9:41155811
|
C | T | 54 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.764+572G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155811 | ||||||
| chr9:41155831
|
G | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.764+552C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155831 | ||||||
| chr9:41155918
|
G | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.764+465C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155918 | ||||||
| chr9:41155997
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.764+386A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155997 | ||||||
| chr9:41155998
|
A | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.764+385T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41155998 | ||||||
| chr9:41156005
|
T | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.764+378A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156005 | ||||||
| chr9:41156081
|
A | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+302T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156081 | ||||||
| chr9:41156160
|
A | G | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.764+223T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156160 | ||||||
| chr9:41156189
|
C | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+194G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156189 | ||||||
| chr9:41156219
|
C | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+164G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156219 | ||||||
| chr9:41156308
|
G | T | 1 | a0001c0003t0001g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.764+75C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156308 | ||||||
| chr9:41156369
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.764+14G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 10/14 | chr9 | 41156369 | ||||||
| chr9:41156457
|
A | G | 54 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.708-18T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156457 | ||||||
| chr9:41156569
|
G | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-130C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156569 | ||||||
| chr9:41156593
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0151 | 3 | HG02165.hp1 NA18980.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.708-154T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156593 | ||||||
| chr9:41156615
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-176G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156615 | ||||||
| chr9:41156629
|
GT | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-191delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156629 | ||||||
| chr9:41156661
|
G | C | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.708-222C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156661 | ||||||
| chr9:41156730
|
C | A | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.708-291G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156730 | ||||||
| chr9:41156732
|
A | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.708-293T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156732 | ||||||
| chr9:41156769
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0142 | 2 | NA18984.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.708-330T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156769 | ||||||
| chr9:41156818
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.708-379C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156818 | ||||||
| chr9:41156909
|
G | C | 4 | a0002c0004t0001g0193a0002c0004t0001g0194a0002c0004t0001g0195others(1): Show | 4 | HG00408.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-470C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41156909 | ||||||
| chr9:41157011
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 212 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.708-572G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157011 | ||||||
| chr9:41157181
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.708-742C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157181 | ||||||
| chr9:41157183
|
T | C | 2 | a0001c0001t0001g0229a0001c0006t0001g0211 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.708-744A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157183 | ||||||
| chr9:41157188
|
G | A | 1 | a0001c0006t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.708-749C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157188 | ||||||
| chr9:41157197
|
C | T | 5 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.708-758G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157197 | ||||||
| chr9:41157199
|
C | T | 1 | a0001c0006t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.708-760G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157199 | ||||||
| chr9:41157204
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0144 | 3 | HG01074.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.708-765C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157204 | ||||||
| chr9:41157233
|
G | A | 2 | a0003c0005t0001g0035a0003c0005t0001g0036 | 2 | NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.708-794C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157233 | ||||||
| chr9:41157334
|
C | T | 6 | a0001c0003t0001g0245a0001c0003t0001g0247a0001c0003t0001g0252others(3): Show | 6 | HG02148.hp1 NA18948.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-895G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157334 | ||||||
| chr9:41157356
|
C | T | 3 | a0001c0006t0001g0211a0001c0006t0001g0226a0002c0004t0001g0212 | 3 | HG00558.hp2 HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.708-917G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157356 | ||||||
| chr9:41157367
|
A | G | 59 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(56): Show | 61 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.708-928T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157367 | ||||||
| chr9:41157466
|
G | GA | 19 | a0001c0001t0001g0140a0001c0006t0001g0027a0003c0005t0001g0003others(16): Show | 22 | HG01175.hp2 HG01884.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.708-1028dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157466 | ||||||
| chr9:41157466
|
GA | G | 6 | a0001c0001t0001g0227a0001c0002t0001g0054a0001c0006t0001g0023others(3): Show | 6 | HG00423.hp2 HG02055.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-1028delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157466 | ||||||
| chr9:41157641
|
A | AT | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.708-1203dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157641 | ||||||
| chr9:41157642
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.708-1203A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157642 | ||||||
| chr9:41157689
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.708-1250T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157689 | ||||||
| chr9:41157735
|
C | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0112others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-1296G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157735 | ||||||
| chr9:41157784
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0090 | 2 | HG01109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.708-1345C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157784 | ||||||
| chr9:41157785
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.708-1346G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157785 | ||||||
| chr9:41157861
|
C | G | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.708-1422G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157861 | ||||||
| chr9:41157947
|
G | A | 39 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0237others(36): Show | 41 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.708-1508C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157947 | ||||||
| chr9:41157981
|
C | T | 32 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(29): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.708-1542G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41157981 | ||||||
| chr9:41158125
|
G | A | 50 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(47): Show | 52 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.708-1686C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158125 | ||||||
| chr9:41158206
|
CG | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.708-1768delC | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158206 | ||||||
| chr9:41158232
|
T | G | 1 | a0001c0006t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.708-1793A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158232 | ||||||
| chr9:41158325
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.708-1886T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158325 | ||||||
| chr9:41158361
|
A | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0007c0012t0001g0180 | 3 | HG02109.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.708-1922T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158361 | ||||||
| chr9:41158393
|
C | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.708-1954G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158393 | ||||||
| chr9:41158475
|
T | C | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.708-2036A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158475 | ||||||
| chr9:41158669
|
C | T | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.708-2230G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158669 | ||||||
| chr9:41158716
|
C | A | 2 | a0002c0004t0001g0205a0002c0004t0001g0208 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.708-2277G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158716 | ||||||
| chr9:41158835
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.708-2396G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158835 | ||||||
| chr9:41158870
|
G | GA | 23 | a0001c0001t0001g0081a0001c0001t0001g0097a0001c0001t0001g0103others(20): Show | 23 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-2432dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158870 | ||||||
| chr9:41158870
|
GA | G | 44 | a0001c0001t0001g0149a0001c0003t0001g0018a0001c0003t0001g0019others(41): Show | 47 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.708-2432delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158870 | ||||||
| chr9:41158935
|
T | C | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.708-2496A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41158935 | ||||||
| chr9:41159130
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.708-2691C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159130 | ||||||
| chr9:41159148
|
A | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0121 | 2 | HG00438.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.708-2709T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159148 | ||||||
| chr9:41159238
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.708-2799G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159238 | ||||||
| chr9:41159274
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.708-2835C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159274 | ||||||
| chr9:41159305
|
G | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-2866C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159305 | ||||||
| chr9:41159324
|
G | C | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.708-2885C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159324 | ||||||
| chr9:41159386
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.707+2947G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159386 | ||||||
| chr9:41159397
|
A | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.707+2936T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159397 | ||||||
| chr9:41159407
|
A | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.707+2926T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159407 | ||||||
| chr9:41159428
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.707+2905C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159428 | ||||||
| chr9:41159474
|
T | C | 6 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+2859A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159474 | ||||||
| chr9:41159482
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.707+2851A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159482 | ||||||
| chr9:41159487
|
C | G | 38 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0237others(35): Show | 40 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.707+2846G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159487 | ||||||
| chr9:41159501
|
G | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.707+2832C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159501 | ||||||
| chr9:41159579
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.707+2754C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159579 | ||||||
| chr9:41159934
|
A | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.707+2399T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41159934 | ||||||
| chr9:41160185
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.707+2148G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160185 | ||||||
| chr9:41160264
|
C | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.707+2069G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160264 | ||||||
| chr9:41160339
|
T | A | 1 | a0001c0002t0001g0273 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.707+1994A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160339 | ||||||
| chr9:41160372
|
T | C | 3 | a0002c0004t0001g0204a0002c0004t0005g0200a0002c0004t0005g0223 | 3 | HG00597.hp1 HG01943.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.707+1961A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160372 | ||||||
| chr9:41160408
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.707+1925G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160408 | ||||||
| chr9:41160426
|
G | GT | 5 | a0002c0004t0001g0193a0002c0004t0001g0194a0002c0004t0001g0195others(2): Show | 5 | HG00408.hp2 HG02080.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.707+1906dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160426 | ||||||
| chr9:41160429
|
TG | T | 96 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(93): Show | 101 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.707+1903delC | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160429 | ||||||
| chr9:41160430
|
G | T | 73 | a0001c0002t0001g0174a0001c0003t0001g0243a0001c0003t0001g0244others(70): Show | 78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.707+1903C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160430 | ||||||
| chr9:41160430
|
GT | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.707+1902delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160430 | ||||||
| chr9:41160435
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.707+1898A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160435 | ||||||
| chr9:41160516
|
G | A | 58 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.707+1817C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160516 | ||||||
| chr9:41160657
|
C | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.707+1676G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160657 | ||||||
| chr9:41160665
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.707+1668C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160665 | ||||||
| chr9:41160689
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+1644A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160689 | ||||||
| chr9:41160692
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.707+1641C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160692 | ||||||
| chr9:41160702
|
G | A | 1 | a0002c0004t0001g0207 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.707+1631C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160702 | ||||||
| chr9:41160713
|
C | T | 1 | a0001c0006t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.707+1620G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160713 | ||||||
| chr9:41160714
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.707+1619C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160714 | ||||||
| chr9:41160830
|
C | T | 5 | a0002c0004t0001g0186a0002c0004t0001g0187a0002c0004t0001g0231others(2): Show | 5 | HG00673.hp1 HG02027.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.707+1503G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160830 | ||||||
| chr9:41160983
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.707+1350G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41160983 | ||||||
| chr9:41161055
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.707+1278C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161055 | ||||||
| chr9:41161177
|
C | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.707+1156G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161177 | ||||||
| chr9:41161178
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.707+1155C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161178 | ||||||
| chr9:41161387
|
C | T | 102 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(99): Show | 106 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.707+946G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161387 | ||||||
| chr9:41161445
|
C | T | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.707+888G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161445 | ||||||
| chr9:41161680
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.707+653G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161680 | ||||||
| chr9:41161733
|
C | CA | 23 | a0001c0002t0001g0031a0001c0002t0001g0033a0001c0002t0001g0176others(20): Show | 26 | HG02083.hp1 HG02486.hp2 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.707+599dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
C | CAA | 27 | a0001c0002t0001g0015a0001c0002t0001g0028a0001c0002t0001g0029others(24): Show | 28 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.707+598_707+599dup others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
C | CAAA | 9 | a0001c0002t0001g0014a0001c0002t0001g0030a0001c0002t0001g0159others(6): Show | 10 | HG02074.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.707+597_707+599dup others(3): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
C | CAAAAA | 6 | a0001c0002t0001g0052a0001c0002t0001g0058a0001c0002t0001g0063others(3): Show | 6 | HG01496.hp1 HG02040.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+595_707+599dup others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
C | CAAAAAA | 9 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(6): Show | 9 | HG02886.hp2 HG03209.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+594_707+599dup others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
CA | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0081others(44): Show | 51 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.707+599delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
CAA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 131 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.707+598_707+599del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161733
|
CAAA | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0123others(3): Show | 6 | HG02109.hp1 NA18944.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.707+597_707+599del others(3): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161733 | ||||||
| chr9:41161758
|
A | T | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.707+575T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161758 | ||||||
| chr9:41161916
|
A | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.707+417T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161916 | ||||||
| chr9:41161934
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.707+399T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161934 | ||||||
| chr9:41161942
|
T | C | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.707+391A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41161942 | ||||||
| chr9:41162229
|
A | C | 1 | a0001c0006t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.707+104T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41162229 | ||||||
| chr9:41162283
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.707+50A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41162283 | ||||||
| chr9:41162329
|
G | A | 1 | a0002c0004t0001g0184 | 1 | HG02630.hp1 | splice_region_variant&intron_variant | LOW | c.707+4C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 9/14 | chr9 | 41162329 | ||||||
| chr9:41162434
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.663-57T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162434 | ||||||
| chr9:41162465
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.663-88G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162465 | ||||||
| chr9:41162467
|
G | A | 1 | a0002c0004t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.663-90C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162467 | ||||||
| chr9:41162639
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 230 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.663-262T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162639 | ||||||
| chr9:41162639
|
A | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.663-262T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162639 | ||||||
| chr9:41162662
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.663-285G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162662 | ||||||
| chr9:41162836
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0148 | 2 | NA18948.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.663-459G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162836 | ||||||
| chr9:41162873
|
C | T | 38 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0237others(35): Show | 40 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.663-496G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162873 | ||||||
| chr9:41162927
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.663-550C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162927 | ||||||
| chr9:41162982
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.663-605C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41162982 | ||||||
| chr9:41163266
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.663-889G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163266 | ||||||
| chr9:41163312
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 159 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.663-935G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163312 | ||||||
| chr9:41163480
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.663-1103G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163480 | ||||||
| chr9:41163624
|
C | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-1247G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163624 | ||||||
| chr9:41163633
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-1256A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163633 | ||||||
| chr9:41163650
|
A | G | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-1273T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163650 | ||||||
| chr9:41163750
|
T | C | 1 | a0002c0004t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.662+1251A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163750 | ||||||
| chr9:41163783
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.662+1218A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163783 | ||||||
| chr9:41163828
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.662+1173C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163828 | ||||||
| chr9:41163906
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.662+1095G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163906 | ||||||
| chr9:41163907
|
G | A | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.662+1094C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41163907 | ||||||
| chr9:41164044
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+957T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164044 | ||||||
| chr9:41164063
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.662+938A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164063 | ||||||
| chr9:41164110
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.662+891G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164110 | ||||||
| chr9:41164169
|
C | T | 55 | a0001c0001t0001g0227a0001c0002t0001g0014a0001c0002t0001g0015others(52): Show | 57 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.662+832G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164169 | ||||||
| chr9:41164170
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0148a0002c0004t0001g0207 | 3 | HG02293.hp1 NA18948.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.662+831C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164170 | ||||||
| chr9:41164170
|
G | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.662+831C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164170 | ||||||
| chr9:41164375
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 285 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.662+626G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164375 | ||||||
| chr9:41164390
|
T | C | 1 | a0002c0004t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.662+611A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164390 | ||||||
| chr9:41164472
|
C | G | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662+529G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164472 | ||||||
| chr9:41164584
|
T | TA | 17 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0117others(14): Show | 17 | HG01175.hp1 HG01257.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.662+416dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164584 | ||||||
| chr9:41164584
|
T | TAA | 194 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.662+415_662+416dup others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164584 | ||||||
| chr9:41164584
|
T | TAAA | 7 | a0001c0001t0001g0098a0001c0001t0001g0150a0001c0003t0001g0237others(4): Show | 7 | HG00741.hp2 HG01106.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.662+414_662+416dup others(3): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164584 | ||||||
| chr9:41164629
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.662+372C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164629 | ||||||
| chr9:41164766
|
G | A | 1 | a0001c0002t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.662+235C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164766 | ||||||
| chr9:41164857
|
C | G | 1 | a0001c0003t0001g0263 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.662+144G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164857 | ||||||
| chr9:41164871
|
T | A | 1 | a0001c0006t0001g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.662+130A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 8/14 | chr9 | 41164871 | ||||||
| chr9:41165137
|
C | T | 2 | a0001c0001t0001g0106a0001c0003t0001g0242 | 2 | HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.576-50G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165137 | ||||||
| chr9:41165196
|
C | A | 1 | a0007c0012t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.576-109G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165196 | ||||||
| chr9:41165231
|
T | C | 1 | a0002c0004t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.576-144A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165231 | ||||||
| chr9:41165236
|
C | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-149G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165236 | ||||||
| chr9:41165261
|
C | T | 2 | a0001c0006t0001g0023a0001c0006t0007g0024 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.576-174G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165261 | ||||||
| chr9:41165269
|
G | A | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034 | 3 | HG02451.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.576-182C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165269 | ||||||
| chr9:41165305
|
T | C | 1 | a0002c0004t0001g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.576-218A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165305 | ||||||
| chr9:41165374
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0121a0001c0001t0001g0128 | 3 | HG00438.hp1 NA18954.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.576-287A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165374 | ||||||
| chr9:41165416
|
G | T | 2 | a0001c0003t0001g0246a0001c0003t0001g0262 | 2 | HG02071.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.576-329C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165416 | ||||||
| chr9:41165506
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.576-419T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165506 | ||||||
| chr9:41165520
|
C | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-433G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165520 | ||||||
| chr9:41165652
|
G | C | 2 | a0001c0002t0001g0055a0001c0002t0001g0056 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.576-565C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165652 | ||||||
| chr9:41165681
|
G | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0097a0001c0001t0001g0103others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.576-594C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165681 | ||||||
| chr9:41165692
|
G | T | 2 | a0001c0002t0001g0070a0001c0002t0001g0273 | 2 | HG01175.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.576-605C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165692 | ||||||
| chr9:41165857
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.576-770T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165857 | ||||||
| chr9:41165883
|
T | C | 3 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0056 | 3 | HG00423.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.576-796A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165883 | ||||||
| chr9:41165888
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.576-801T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165888 | ||||||
| chr9:41165939
|
T | C | 2 | a0001c0003t0004g0235a0006c0011t0004g0234 | 2 | HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.575+845A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165939 | ||||||
| chr9:41165951
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0114a0001c0001t0001g0144 | 3 | HG01074.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.575+833G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165951 | ||||||
| chr9:41165964
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.575+820T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41165964 | ||||||
| chr9:41166011
|
T | C | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.575+773A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166011 | ||||||
| chr9:41166093
|
A | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.575+691T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166093 | ||||||
| chr9:41166122
|
C | T | 1 | a0002c0004t0001g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.575+662G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166122 | ||||||
| chr9:41166123
|
G | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.575+661C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166123 | ||||||
| chr9:41166169
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.575+615C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166169 | ||||||
| chr9:41166204
|
G | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.575+580C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166204 | ||||||
| chr9:41166265
|
A | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273others(1): Show | 4 | HG01109.hp2 HG01175.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+519T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166265 | ||||||
| chr9:41166298
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099 | 5 | HG00438.hp2 HG00597.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+486C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166298 | ||||||
| chr9:41166343
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.575+441G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166343 | ||||||
| chr9:41166376
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+408G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166376 | ||||||
| chr9:41166429
|
A | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0150a0001c0002t0001g0178others(3): Show | 6 | HG00741.hp1 HG01106.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.575+355T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166429 | ||||||
| chr9:41166432
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 178 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.575+352T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166432 | ||||||
| chr9:41166435
|
T | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+349A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166435 | ||||||
| chr9:41166445
|
C | CAT | 5 | a0001c0001t0001g0138a0001c0002t0001g0029a0001c0002t0001g0176others(2): Show | 5 | HG02280.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.575+337_575+338dup others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166445 | ||||||
| chr9:41166445
|
CAT | C | 84 | a0001c0001t0001g0089a0001c0001t0001g0112a0001c0001t0001g0128others(81): Show | 89 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.575+337_575+338del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166445 | ||||||
| chr9:41166445
|
CATAT | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.575+335_575+338del others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166445 | ||||||
| chr9:41166445
|
CATATAT | C | 17 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0001g0117others(14): Show | 18 | HG01255.hp1 HG01257.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.575+333_575+338del others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166445 | ||||||
| chr9:41166445
|
CATATATA others(5): Show |
C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+327_575+338del others(12): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166445 | ||||||
| chr9:41166473
|
T | A | 43 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(40): Show | 46 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.575+311A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166473 | ||||||
| chr9:41166517
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+267A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166517 | ||||||
| chr9:41166560
|
C | G | 1 | a0001c0003t0001g0019 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.575+224G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166560 | ||||||
| chr9:41166586
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+198G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166586 | ||||||
| chr9:41166729
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.575+55A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166729 | ||||||
| chr9:41166745
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+39C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166745 | ||||||
| chr9:41166753
|
A | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.575+31T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 7/14 | chr9 | 41166753 | ||||||
| chr9:41166871
|
T | A | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0007c0012t0001g0180 | 3 | HG02109.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.529-41A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41166871 | ||||||
| chr9:41167005
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-175G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167005 | ||||||
| chr9:41167119
|
TTCACATA others(3): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.529-299_529-290del others(10): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167119 | ||||||
| chr9:41167197
|
C | G | 1 | a0001c0002t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.529-367G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167197 | ||||||
| chr9:41167224
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-394T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167224 | ||||||
| chr9:41167315
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-485T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167315 | ||||||
| chr9:41167379
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.529-549G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167379 | ||||||
| chr9:41167427
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.529-597G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167427 | ||||||
| chr9:41167459
|
T | C | 2 | a0001c0006t0001g0211a0001c0006t0001g0226 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.529-629A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167459 | ||||||
| chr9:41167588
|
T | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.529-758A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167588 | ||||||
| chr9:41167601
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-771G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167601 | ||||||
| chr9:41167697
|
T | A | 54 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.529-867A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167697 | ||||||
| chr9:41167869
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1039G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167869 | ||||||
| chr9:41167938
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1108C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167938 | ||||||
| chr9:41167993
|
C | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.529-1163G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41167993 | ||||||
| chr9:41168040
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1210G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168040 | ||||||
| chr9:41168176
|
C | A | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.529-1346G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168176 | ||||||
| chr9:41168177
|
A | G | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.529-1347T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168177 | ||||||
| chr9:41168178
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1348T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168178 | ||||||
| chr9:41168203
|
C | T | 1 | a0001c0003t0001g0263 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.529-1373G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168203 | ||||||
| chr9:41168269
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0143 | 2 | HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.529-1439C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168269 | ||||||
| chr9:41168270
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0143 | 2 | HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.529-1440G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168270 | ||||||
| chr9:41168274
|
G | A | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.529-1444C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168274 | ||||||
| chr9:41168297
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.529-1467A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168297 | ||||||
| chr9:41168318
|
C | A | 55 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(52): Show | 57 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.529-1488G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168318 | ||||||
| chr9:41168430
|
T | TACA | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.529-1603_529-1601d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168430 | ||||||
| chr9:41168639
|
A | T | 1 | a0001c0002t0001g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.529-1809T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168639 | ||||||
| chr9:41168654
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529-1824A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168654 | ||||||
| chr9:41168657
|
T | G | 59 | a0001c0001t0001g0080a0001c0002t0001g0014a0001c0002t0001g0015others(56): Show | 61 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.529-1827A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168657 | ||||||
| chr9:41168724
|
G | A | 1 | a0003c0005t0001g0005 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.529-1894C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168724 | ||||||
| chr9:41168795
|
G | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.529-1965C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168795 | ||||||
| chr9:41168887
|
A | C | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.529-2057T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41168887 | ||||||
| chr9:41169056
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2226A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169056 | ||||||
| chr9:41169099
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2269T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169099 | ||||||
| chr9:41169102
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2272C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169102 | ||||||
| chr9:41169119
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.529-2289A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169119 | ||||||
| chr9:41169161
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.529-2331T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169161 | ||||||
| chr9:41169222
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2392T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169222 | ||||||
| chr9:41169372
|
A | AT | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.529-2543dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169372 | ||||||
| chr9:41169392
|
T | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2562A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169392 | ||||||
| chr9:41169718
|
G | T | 1 | a0002c0004t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.529-2888C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169718 | ||||||
| chr9:41169738
|
C | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2908G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169738 | ||||||
| chr9:41169757
|
C | T | 2 | a0001c0003t0004g0235a0006c0011t0004g0234 | 2 | HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.529-2927G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169757 | ||||||
| chr9:41169774
|
T | TAGGTTAA others(8): Show |
4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2937_528+2938i others(17): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169774 | ||||||
| chr9:41169776
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2936T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169776 | ||||||
| chr9:41169798
|
C | T | 1 | a0002c0004t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.528+2914G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169798 | ||||||
| chr9:41169823
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.528+2889A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169823 | ||||||
| chr9:41169859
|
G | T | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.528+2853C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169859 | ||||||
| chr9:41169861
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.528+2851A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169861 | ||||||
| chr9:41169865
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2847T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169865 | ||||||
| chr9:41169924
|
C | T | 1 | a0002c0004t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.528+2788G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169924 | ||||||
| chr9:41169927
|
T | C | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.528+2785A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169927 | ||||||
| chr9:41169969
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.528+2743C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169969 | ||||||
| chr9:41169998
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.528+2714G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169998 | ||||||
| chr9:41169999
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.528+2713A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41169999 | ||||||
| chr9:41170000
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2712T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170000 | ||||||
| chr9:41170041
|
C | A | 1 | a0002c0004t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.528+2671G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170041 | ||||||
| chr9:41170112
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0082others(2): Show | 5 | NA18944.hp2 NA18984.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+2600A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170112 | ||||||
| chr9:41170121
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.528+2591C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170121 | ||||||
| chr9:41170367
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+2345G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170367 | ||||||
| chr9:41170467
|
C | T | 4 | a0002c0004t0001g0193a0002c0004t0001g0194a0002c0004t0001g0195others(1): Show | 4 | HG00408.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2245G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170467 | ||||||
| chr9:41170546
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+2166T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170546 | ||||||
| chr9:41170787
|
C | T | 54 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.528+1925G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170787 | ||||||
| chr9:41170788
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+1924T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170788 | ||||||
| chr9:41170847
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.528+1865C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170847 | ||||||
| chr9:41170878
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.528+1834G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170878 | ||||||
| chr9:41170883
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+1829G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41170883 | ||||||
| chr9:41171022
|
T | TA | 45 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(42): Show | 48 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.528+1689dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171022 | ||||||
| chr9:41171152
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.528+1560A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171152 | ||||||
| chr9:41171174
|
G | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1538C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171174 | ||||||
| chr9:41171283
|
G | T | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.528+1429C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171283 | ||||||
| chr9:41171304
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+1408G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171304 | ||||||
| chr9:41171329
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1383G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171329 | ||||||
| chr9:41171346
|
C | T | 1 | a0001c0006t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.528+1366G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171346 | ||||||
| chr9:41171347
|
G | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0056 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.528+1365C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171347 | ||||||
| chr9:41171400
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1312T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171400 | ||||||
| chr9:41171409
|
TAG | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+1301_528+1302d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171409 | ||||||
| chr9:41171436
|
G | GA | 58 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(55): Show | 60 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.528+1275dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171436 | ||||||
| chr9:41171437
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00544.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.528+1275T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171437 | ||||||
| chr9:41171513
|
A | T | 54 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.528+1199T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171513 | ||||||
| chr9:41171517
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1195G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171517 | ||||||
| chr9:41171552
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+1160G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171552 | ||||||
| chr9:41171632
|
T | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.528+1080A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171632 | ||||||
| chr9:41171673
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1039C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171673 | ||||||
| chr9:41171723
|
C | T | 2 | a0003c0005t0001g0035a0003c0005t0001g0036 | 2 | NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.528+989G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171723 | ||||||
| chr9:41171750
|
C | CA | 58 | a0001c0001t0001g0138a0001c0001t0001g0142a0001c0002t0001g0230others(55): Show | 60 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.528+961dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171750 | ||||||
| chr9:41171750
|
CA | C | 56 | a0001c0001t0001g0102a0001c0001t0001g0127a0001c0001t0001g0131others(53): Show | 58 | HG00423.hp2 HG00733.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.528+961delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171750 | ||||||
| chr9:41171774
|
C | T | 7 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(4): Show | 7 | HG00673.hp1 HG02109.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+938G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171774 | ||||||
| chr9:41171796
|
C | T | 1 | a0001c0002t0001g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.528+916G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171796 | ||||||
| chr9:41171804
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+908T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171804 | ||||||
| chr9:41171883
|
G | A | 1 | a0002c0004t0001g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.528+829C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171883 | ||||||
| chr9:41171901
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+811T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171901 | ||||||
| chr9:41171952
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+760T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171952 | ||||||
| chr9:41171953
|
T | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.528+759A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41171953 | ||||||
| chr9:41172091
|
T | C | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.528+621A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172091 | ||||||
| chr9:41172147
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0101 | 2 | NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.528+565G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172147 | ||||||
| chr9:41172151
|
T | A | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.528+561A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172151 | ||||||
| chr9:41172249
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.528+463C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172249 | ||||||
| chr9:41172250
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+462C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172250 | ||||||
| chr9:41172257
|
T | G | 7 | a0003c0005t0001g0003a0003c0005t0001g0005a0003c0005t0001g0040others(4): Show | 9 | NA18944.hp1 NA18949.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+455A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172257 | ||||||
| chr9:41172337
|
G | C | 54 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.528+375C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172337 | ||||||
| chr9:41172368
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.528+344C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172368 | ||||||
| chr9:41172410
|
C | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+302G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172410 | ||||||
| chr9:41172546
|
C | G | 1 | a0001c0002t0001g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.528+166G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172546 | ||||||
| chr9:41172615
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+97T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172615 | ||||||
| chr9:41172626
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+86C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172626 | ||||||
| chr9:41172654
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 212 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.528+58G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 6/14 | chr9 | 41172654 | ||||||
| chr9:41172750
|
C | T | 2 | a0001c0002t0001g0159a0001c0002t0001g0163 | 2 | NA19001.hp2 NA19085.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.491-1G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41172750 | ||||||
| chr9:41172895
|
G | T | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.491-146C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41172895 | ||||||
| chr9:41173046
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-297G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173046 | ||||||
| chr9:41173172
|
C | A | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.491-423G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173172 | ||||||
| chr9:41173216
|
A | T | 1 | a0001c0003t0001g0242 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.491-467T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173216 | ||||||
| chr9:41173269
|
C | A | 1 | a0001c0006t0002g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.491-520G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173269 | ||||||
| chr9:41173335
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.491-586G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173335 | ||||||
| chr9:41173358
|
C | T | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.491-609G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173358 | ||||||
| chr9:41173554
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.490+739G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173554 | ||||||
| chr9:41173653
|
T | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+640A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173653 | ||||||
| chr9:41173676
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+617A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173676 | ||||||
| chr9:41173684
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+609C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173684 | ||||||
| chr9:41173725
|
AT | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(221): Show | 241 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.490+567delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173725 | ||||||
| chr9:41173725
|
ATT | A | 40 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(37): Show | 43 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.490+566_490+567del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173725 | ||||||
| chr9:41173728
|
T | G | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0007c0012t0001g0180 | 3 | HG02109.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.490+565A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173728 | ||||||
| chr9:41173729
|
T | G | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490+564A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173729 | ||||||
| chr9:41173733
|
T | C | 2 | a0004c0007t0001g0277a0004c0007t0001g0278 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.490+560A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173733 | ||||||
| chr9:41173860
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+433T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173860 | ||||||
| chr9:41173886
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+407A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173886 | ||||||
| chr9:41173908
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+385G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173908 | ||||||
| chr9:41173977
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.490+316A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173977 | ||||||
| chr9:41173988
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+305T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41173988 | ||||||
| chr9:41174043
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+250T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174043 | ||||||
| chr9:41174094
|
C | T | 54 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.490+199G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174094 | ||||||
| chr9:41174115
|
G | A | 46 | a0001c0002t0001g0230a0002c0004t0001g0016a0002c0004t0001g0017others(43): Show | 48 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.490+178C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174115 | ||||||
| chr9:41174158
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.490+135C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174158 | ||||||
| chr9:41174232
|
G | GA | 29 | a0001c0002t0001g0071a0001c0003t0001g0258a0001c0003t0001g0265others(26): Show | 32 | HG00673.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.490+60dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
G | GAA | 9 | a0001c0001t0001g0130a0001c0002t0001g0070a0001c0002t0001g0273others(6): Show | 9 | HG01175.hp1 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+59_490+60dupTT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
G | GAAA | 63 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 71 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.490+58_490+60dupTT others(1): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
G | GAAAA | 31 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0086others(28): Show | 33 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+57_490+60dupTT others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
GA | G | 30 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(27): Show | 33 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.490+60delT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
GAAAAA | G | 11 | a0001c0002t0001g0029a0001c0002t0001g0069a0001c0002t0001g0159others(8): Show | 11 | HG01928.hp1 HG02055.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+56_490+60delTT others(3): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174232
|
GAAAAAA | G | 42 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(39): Show | 44 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+55_490+60delTT others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174232 | ||||||
| chr9:41174241
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+52T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174241 | ||||||
| chr9:41174244
|
A | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.490+49T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174244 | ||||||
| chr9:41174246
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+47T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 5/14 | chr9 | 41174246 | ||||||
| chr9:41174396
|
T | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-44A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174396 | ||||||
| chr9:41174503
|
T | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-151A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174503 | ||||||
| chr9:41174677
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0082others(1): Show | 4 | NA18984.hp2 NA18986.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-325C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174677 | ||||||
| chr9:41174822
|
T | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-470A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174822 | ||||||
| chr9:41174832
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.431-480A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174832 | ||||||
| chr9:41174874
|
A | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 111 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.431-522T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174874 | ||||||
| chr9:41174894
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.431-542T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174894 | ||||||
| chr9:41174950
|
A | G | 1 | a0002c0004t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-598T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174950 | ||||||
| chr9:41174994
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.431-642C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41174994 | ||||||
| chr9:41175045
|
A | G | 1 | a0001c0002t0001g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.431-693T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175045 | ||||||
| chr9:41175051
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.431-699A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175051 | ||||||
| chr9:41175106
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-754T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175106 | ||||||
| chr9:41175146
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-794T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175146 | ||||||
| chr9:41175217
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-865T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175217 | ||||||
| chr9:41175219
|
G | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-867C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175219 | ||||||
| chr9:41175313
|
G | A | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.431-961C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175313 | ||||||
| chr9:41175313
|
G | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-961C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175313 | ||||||
| chr9:41175342
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-990C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175342 | ||||||
| chr9:41175408
|
T | G | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.431-1056A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175408 | ||||||
| chr9:41175452
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1100T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175452 | ||||||
| chr9:41175476
|
C | T | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1124G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175476 | ||||||
| chr9:41175488
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-1136A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175488 | ||||||
| chr9:41175501
|
G | A | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1149C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175501 | ||||||
| chr9:41175797
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-1445A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175797 | ||||||
| chr9:41175828
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0128 | 2 | NA18964.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.431-1476T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175828 | ||||||
| chr9:41175840
|
T | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0128a0001c0002t0001g0178others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1488A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175840 | ||||||
| chr9:41175907
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-1555C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175907 | ||||||
| chr9:41175910
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.431-1558G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175910 | ||||||
| chr9:41175937
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.431-1585A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41175937 | ||||||
| chr9:41176040
|
A | T | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.431-1688T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176040 | ||||||
| chr9:41176094
|
AC | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1743delG | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176094 | ||||||
| chr9:41176102
|
T | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1750A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176102 | ||||||
| chr9:41176104
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1752T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176104 | ||||||
| chr9:41176179
|
G | A | 1 | a0001c0001t0001g0013 | 2 | NA18939.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.431-1827C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176179 | ||||||
| chr9:41176253
|
G | A | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1901C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176253 | ||||||
| chr9:41176314
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.431-1962T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176314 | ||||||
| chr9:41176352
|
G | C | 3 | a0001c0001t0001g0095a0001c0003t0001g0237a0001c0003t0001g0238 | 3 | HG00741.hp2 HG03942.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.431-2000C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176352 | ||||||
| chr9:41176374
|
T | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0149 | 3 | HG01167.hp1 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.431-2022A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176374 | ||||||
| chr9:41176425
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.431-2073C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176425 | ||||||
| chr9:41176512
|
A | C | 1 | a0002c0004t0001g0016 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.431-2160T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176512 | ||||||
| chr9:41176517
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.431-2165A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176517 | ||||||
| chr9:41176533
|
G | A | 3 | a0001c0002t0001g0058a0001c0002t0001g0065a0001c0002t0001g0066 | 3 | HG01496.hp1 HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.431-2181C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176533 | ||||||
| chr9:41176618
|
C | T | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-2266G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176618 | ||||||
| chr9:41176668
|
A | G | 3 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0056 | 3 | HG00423.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.431-2316T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176668 | ||||||
| chr9:41176690
|
T | A | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2338A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176690 | ||||||
| chr9:41176721
|
ACATAGAA others(7): Show |
A | 1 | a0001c0002t0001g0015 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.431-2383_431-2370d others(16): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176721 | ||||||
| chr9:41176776
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-2424C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176776 | ||||||
| chr9:41176788
|
T | C | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-2436A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176788 | ||||||
| chr9:41176853
|
G | A | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-2501C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176853 | ||||||
| chr9:41176861
|
G | GAACC | 5 | a0001c0001t0001g0095a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-2513_431-2510d others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176861 | ||||||
| chr9:41176956
|
T | A | 1 | a0001c0002t0001g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.431-2604A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41176956 | ||||||
| chr9:41177025
|
G | A | 54 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(51): Show | 56 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.431-2673C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177025 | ||||||
| chr9:41177035
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2683T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177035 | ||||||
| chr9:41177039
|
C | CCAATTAA others(78): Show |
1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2688_431-2687i others(87): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177039 | ||||||
| chr9:41177054
|
T | C | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.431-2702A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177054 | ||||||
| chr9:41177087
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2735A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177087 | ||||||
| chr9:41177107
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2755A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177107 | ||||||
| chr9:41177160
|
A | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-2808T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177160 | ||||||
| chr9:41177348
|
G | A | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-2996C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177348 | ||||||
| chr9:41177405
|
T | C | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG00741.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.431-3053A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177405 | ||||||
| chr9:41177460
|
T | C | 1 | a0001c0006t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.431-3108A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177460 | ||||||
| chr9:41177550
|
C | T | 3 | a0001c0003t0001g0020a0001c0003t0001g0264a0001c0003t0001g0265 | 4 | HG01243.hp2 HG01928.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-3198G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177550 | ||||||
| chr9:41177577
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-3225G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177577 | ||||||
| chr9:41177703
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.431-3351A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177703 | ||||||
| chr9:41177715
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-3363T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177715 | ||||||
| chr9:41177750
|
T | A | 6 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-3398A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177750 | ||||||
| chr9:41177750
|
T | G | 51 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(48): Show | 53 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.431-3398A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177750 | ||||||
| chr9:41177896
|
C | T | 1 | a0002c0004t0001g0188 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.431-3544G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177896 | ||||||
| chr9:41177915
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.431-3563C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41177915 | ||||||
| chr9:41178003
|
G | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.431-3651C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178003 | ||||||
| chr9:41178215
|
C | T | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.431-3863G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178215 | ||||||
| chr9:41178285
|
T | C | 1 | a0001c0002t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.431-3933A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178285 | ||||||
| chr9:41178294
|
C | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-3942G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178294 | ||||||
| chr9:41178353
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.431-4001T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178353 | ||||||
| chr9:41178414
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3961A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178414 | ||||||
| chr9:41178464
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3911T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178464 | ||||||
| chr9:41178503
|
C | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+3872G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178503 | ||||||
| chr9:41178528
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3847T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178528 | ||||||
| chr9:41178548
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3827G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178548 | ||||||
| chr9:41178561
|
T | A | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3814A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178561 | ||||||
| chr9:41178668
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.430+3707C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178668 | ||||||
| chr9:41178780
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.430+3595G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178780 | ||||||
| chr9:41178788
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3587T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178788 | ||||||
| chr9:41178855
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+3520G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178855 | ||||||
| chr9:41178905
|
G | GGAA | 43 | a0001c0001t0001g0095a0001c0003t0001g0018a0001c0003t0001g0019others(40): Show | 46 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.430+3467_430+3469d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41178905 | ||||||
| chr9:41179060
|
A | G | 1 | a0001c0003t0001g0241 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.430+3315T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179060 | ||||||
| chr9:41179161
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+3214A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179161 | ||||||
| chr9:41179220
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+3155T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179220 | ||||||
| chr9:41179278
|
T | G | 53 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(50): Show | 55 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.430+3097A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179278 | ||||||
| chr9:41179345
|
T | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.430+3030A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179345 | ||||||
| chr9:41179408
|
G | A | 1 | a0001c0003t0001g0259 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.430+2967C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179408 | ||||||
| chr9:41179465
|
C | G | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+2910G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179465 | ||||||
| chr9:41179495
|
A | T | 1 | a0001c0002t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430+2880T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179495 | ||||||
| chr9:41179563
|
C | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.430+2812G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179563 | ||||||
| chr9:41179604
|
C | A | 1 | a0008c0010t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.430+2771G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179604 | ||||||
| chr9:41179635
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+2740G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179635 | ||||||
| chr9:41179685
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.430+2690G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179685 | ||||||
| chr9:41179797
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.430+2578A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179797 | ||||||
| chr9:41179860
|
T | C | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0079others(19): Show | 24 | HG00423.hp1 HG00544.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.430+2515A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179860 | ||||||
| chr9:41179894
|
A | C | 60 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(57): Show | 62 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.430+2481T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41179894 | ||||||
| chr9:41180084
|
A | C | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.430+2291T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180084 | ||||||
| chr9:41180090
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.430+2285A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180090 | ||||||
| chr9:41180105
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.430+2270A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180105 | ||||||
| chr9:41180168
|
C | CT | 12 | a0001c0002t0001g0070a0001c0002t0001g0163a0001c0003t0001g0018others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+2206dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180168 | ||||||
| chr9:41180168
|
C | CTT | 90 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(87): Show | 94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.430+2205_430+2206d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180168 | ||||||
| chr9:41180168
|
C | CTTT | 46 | a0001c0002t0001g0059a0001c0002t0001g0069a0001c0002t0001g0158others(43): Show | 48 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.430+2204_430+2206d others(5): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180168 | ||||||
| chr9:41180168
|
CT | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.430+2206delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180168 | ||||||
| chr9:41180168
|
CTT | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0080others(10): Show | 14 | HG00558.hp1 HG01074.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+2205_430+2206d others(4): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180168 | ||||||
| chr9:41180319
|
C | T | 1 | a0002c0004t0001g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.430+2056G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180319 | ||||||
| chr9:41180333
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2042T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180333 | ||||||
| chr9:41180403
|
G | A | 1 | a0002c0004t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+1972C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180403 | ||||||
| chr9:41180434
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0181others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1941G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180434 | ||||||
| chr9:41180474
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+1901A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180474 | ||||||
| chr9:41180500
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1875G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180500 | ||||||
| chr9:41180505
|
G | C | 1 | a0001c0006t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.430+1870C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180505 | ||||||
| chr9:41180544
|
G | T | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+1831C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180544 | ||||||
| chr9:41180660
|
ATGTG | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+1711_430+1714d others(6): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180660 | ||||||
| chr9:41180674
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01123.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.430+1701C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180674 | ||||||
| chr9:41180680
|
G | A | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+1695C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180680 | ||||||
| chr9:41180750
|
G | A | 3 | a0001c0002t0001g0015a0001c0002t0001g0176a0001c0002t0001g0177 | 4 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1625C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180750 | ||||||
| chr9:41180830
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.430+1545C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180830 | ||||||
| chr9:41180867
|
G | T | 1 | a0001c0002t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430+1508C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180867 | ||||||
| chr9:41180882
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0149 | 3 | HG01167.hp1 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.430+1493A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180882 | ||||||
| chr9:41180971
|
A | G | 1 | a0001c0002t0001g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.430+1404T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180971 | ||||||
| chr9:41180975
|
C | G | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.430+1400G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41180975 | ||||||
| chr9:41181050
|
A | C | 2 | a0004c0007t0001g0277a0004c0007t0001g0278 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.430+1325T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181050 | ||||||
| chr9:41181285
|
G | A | 1 | a0001c0001t0001g0013 | 2 | NA18939.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.430+1090C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181285 | ||||||
| chr9:41181322
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.430+1053G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181322 | ||||||
| chr9:41181563
|
G | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+812C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181563 | ||||||
| chr9:41181810
|
C | T | 8 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(5): Show | 8 | HG00423.hp2 HG02886.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+565G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181810 | ||||||
| chr9:41181893
|
T | C | 2 | a0001c0003t0004g0235a0006c0011t0004g0234 | 2 | HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430+482A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181893 | ||||||
| chr9:41181923
|
T | A | 3 | a0002c0004t0001g0017a0002c0004t0001g0224a0002c0004t0001g0225 | 4 | NA18950.hp1 NA18965.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+452A>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41181923 | ||||||
| chr9:41182045
|
G | A | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+330C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41182045 | ||||||
| chr9:41182068
|
G | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+307C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41182068 | ||||||
| chr9:41182075
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.430+300G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41182075 | ||||||
| chr9:41182154
|
C | T | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+221G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 4/14 | chr9 | 41182154 | ||||||
| chr9:41182558
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.339-92C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182558 | ||||||
| chr9:41182669
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.339-203T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182669 | ||||||
| chr9:41182713
|
C | T | 32 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(29): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.339-247G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182713 | ||||||
| chr9:41182762
|
T | G | 96 | a0001c0001t0001g0150a0001c0002t0001g0014a0001c0002t0001g0015others(93): Show | 101 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.339-296A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182762 | ||||||
| chr9:41182902
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0151 | 2 | HG02165.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.339-436A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182902 | ||||||
| chr9:41182988
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.339-522A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41182988 | ||||||
| chr9:41183008
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.339-542G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183008 | ||||||
| chr9:41183027
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00544.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.338+537G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183027 | ||||||
| chr9:41183115
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.338+449T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183115 | ||||||
| chr9:41183218
|
A | AT | 148 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(145): Show | 159 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.338+345dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183218 | ||||||
| chr9:41183218
|
AT | A | 8 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(5): Show | 9 | HG01175.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.338+345delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183218 | ||||||
| chr9:41183230
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.338+334T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183230 | ||||||
| chr9:41183439
|
T | G | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.338+125A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183439 | ||||||
| chr9:41183512
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.338+52A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 3/14 | chr9 | 41183512 | ||||||
| chr9:41183689
|
C | A | 1 | a0002c0004t0001g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.242-29G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41183689 | ||||||
| chr9:41183833
|
C | G | 1 | a0001c0003t0001g0239 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.242-173G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41183833 | ||||||
| chr9:41183896
|
G | A | 1 | a0007c0012t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.242-236C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41183896 | ||||||
| chr9:41183923
|
C | A | 45 | a0002c0004t0001g0016a0002c0004t0001g0017a0002c0004t0001g0184others(42): Show | 47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.242-263G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41183923 | ||||||
| chr9:41184012
|
C | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.242-352G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184012 | ||||||
| chr9:41184018
|
T | G | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.242-358A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184018 | ||||||
| chr9:41184198
|
G | A | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.242-538C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184198 | ||||||
| chr9:41184218
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.242-558T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184218 | ||||||
| chr9:41184255
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.242-595T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184255 | ||||||
| chr9:41184279
|
T | G | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.242-619A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184279 | ||||||
| chr9:41184311
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.242-651C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184311 | ||||||
| chr9:41184428
|
A | T | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.242-768T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184428 | ||||||
| chr9:41184437
|
C | CA | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.242-778dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184437 | ||||||
| chr9:41184598
|
TAA | T | 7 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161others(4): Show | 7 | HG01928.hp1 HG02074.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.242-940_242-939del others(2): Show |
ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184598 | ||||||
| chr9:41184856
|
A | T | 57 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0028others(54): Show | 59 | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.241+1137T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41184856 | ||||||
| chr9:41185041
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241+952C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185041 | ||||||
| chr9:41185071
|
T | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241+922A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185071 | ||||||
| chr9:41185097
|
T | C | 1 | a0002c0004t0005g0223 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.241+896A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185097 | ||||||
| chr9:41185103
|
A | G | 1 | a0006c0011t0004g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.241+890T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185103 | ||||||
| chr9:41185110
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+883G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185110 | ||||||
| chr9:41185144
|
AT | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.241+848delA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185144 | ||||||
| chr9:41185301
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.241+692G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185301 | ||||||
| chr9:41185441
|
G | A | 2 | a0001c0006t0001g0211a0001c0006t0001g0226 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.241+552C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185441 | ||||||
| chr9:41185446
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.241+547C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185446 | ||||||
| chr9:41185490
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.241+503G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185490 | ||||||
| chr9:41185510
|
T | C | 18 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(15): Show | 18 | HG00423.hp2 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.241+483A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185510 | ||||||
| chr9:41185541
|
C | T | 8 | a0002c0004t0001g0017a0002c0004t0001g0186a0002c0004t0001g0187others(5): Show | 9 | HG00673.hp1 HG02027.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+452G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185541 | ||||||
| chr9:41185548
|
C | T | 1 | a0001c0002t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.241+445G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185548 | ||||||
| chr9:41185566
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.241+427C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185566 | ||||||
| chr9:41185597
|
C | T | 2 | a0001c0003t0001g0237a0001c0003t0001g0238 | 2 | HG00741.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.241+396G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185597 | ||||||
| chr9:41185598
|
G | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.241+395C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185598 | ||||||
| chr9:41185602
|
G | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241+391C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185602 | ||||||
| chr9:41185607
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.241+386T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185607 | ||||||
| chr9:41185651
|
A | G | 1 | a0002c0004t0001g0185 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.241+342T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185651 | ||||||
| chr9:41185860
|
C | G | 1 | a0002c0004t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.241+133G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185860 | ||||||
| chr9:41185938
|
G | A | 1 | a0002c0004t0001g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.241+55C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185938 | ||||||
| chr9:41185992
|
C | A | 1 | a0001c0002t0001g0183 | 1 | HG02602.hp2 | splice_donor_variant&intron_variant | HIGH | c.241+1G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 2/14 | chr9 | 41185992 | ||||||
| chr9:41186157
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.155-78T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186157 | ||||||
| chr9:41186185
|
A | G | 2 | a0001c0003t0001g0018a0001c0003t0001g0236 | 3 | HG02280.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.155-106T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186185 | ||||||
| chr9:41186372
|
C | G | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-293G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186372 | ||||||
| chr9:41186448
|
T | C | 1 | a0002c0004t0005g0223 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.155-369A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186448 | ||||||
| chr9:41186694
|
C | CT | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 216 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.155-616dupA | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186694 | ||||||
| chr9:41186736
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18984.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.155-657T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186736 | ||||||
| chr9:41186750
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.155-671T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186750 | ||||||
| chr9:41186944
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-865A>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41186944 | ||||||
| chr9:41187040
|
G | A | 10 | a0001c0003t0001g0020a0001c0003t0001g0264a0001c0003t0001g0265others(7): Show | 11 | HG00639.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-961C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187040 | ||||||
| chr9:41187122
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 108 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.155-1043T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187122 | ||||||
| chr9:41187129
|
G | GA | 5 | a0001c0002t0001g0069a0001c0006t0001g0026a0002c0004t0001g0017others(2): Show | 6 | HG02738.hp1 HG03516.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-1051dupT | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187129 | ||||||
| chr9:41187221
|
G | A | 1 | a0001c0006t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.155-1142C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187221 | ||||||
| chr9:41187305
|
T | G | 1 | a0004c0007t0001g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-1226A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187305 | ||||||
| chr9:41187429
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.155-1350A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187429 | ||||||
| chr9:41187613
|
T | G | 19 | a0001c0002t0001g0228a0003c0005t0001g0003a0003c0005t0001g0004others(16): Show | 22 | HG01175.hp2 HG02083.hp1 HG03139.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+1492A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187613 | ||||||
| chr9:41187771
|
C | A | 1 | a0001c0001t0001g0229 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.154+1334G>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187771 | ||||||
| chr9:41187897
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.154+1208C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41187897 | ||||||
| chr9:41188033
|
C | T | 3 | a0002c0004t0003g0072a0002c0004t0003g0073a0002c0004t0003g0074 | 3 | HG00735.hp1 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.154+1072G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188033 | ||||||
| chr9:41188050
|
A | C | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.154+1055T>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188050 | ||||||
| chr9:41188070
|
A | T | 1 | a0001c0006t0001g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.154+1035T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188070 | ||||||
| chr9:41188119
|
C | G | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0273 | 3 | HG01175.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.154+986G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188119 | ||||||
| chr9:41188339
|
C | G | 19 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(16): Show | 19 | HG00423.hp2 HG01496.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.154+766G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188339 | ||||||
| chr9:41188384
|
G | C | 3 | a0002c0004t0001g0231a0002c0004t0001g0232a0002c0004t0001g0233 | 3 | HG00673.hp1 HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.154+721C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188384 | ||||||
| chr9:41188670
|
A | G | 2 | a0001c0003t0004g0235a0006c0011t0004g0234 | 2 | HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.154+435T>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188670 | ||||||
| chr9:41188700
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(39): Show | 45 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.154+405C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188700 | ||||||
| chr9:41188757
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.154+348C>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188757 | ||||||
| chr9:41188812
|
G | C | 1 | a0001c0002t0001g0273 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.154+293C>G | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188812 | ||||||
| chr9:41188918
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154+187C>T | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188918 | ||||||
| chr9:41188942
|
A | T | 18 | a0003c0005t0001g0003a0003c0005t0001g0004a0003c0005t0001g0005others(15): Show | 21 | HG01175.hp2 HG02083.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+163T>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188942 | ||||||
| chr9:41188974
|
C | G | 8 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+131G>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188974 | ||||||
| chr9:41188974
|
C | T | 4 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(1): Show | 4 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+131G>A | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188974 | ||||||
| chr9:41188982
|
T | G | 2 | a0001c0002t0001g0275a0001c0002t0001g0276 | 2 | HG02074.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.154+123A>C | ZNG1F | ENSG00000215126.12 | transcript | ENST00000377391.8 | protein_coding | 1/14 | chr9 | 41188982 |