Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 150472 |
|---|---|
| ensemblid | ENSG00000136682.16 |
| hgncid | 17907 |
| symbol | ZNG1B |
| name | Zn regulated GTPase metalloprotein activator 1B |
| refseq_nuc | NM_172003.3 |
| refseq_prot | NP_742000.1 |
| ensembl_nuc | ENST00000259199.9 |
| ensembl_prot | ENSP00000259199.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 113437691 |
| end | 113496204 |
| strand | + |
| ver | v1.2 |
| region | chr2:113437691-113496204 |
| region5000 | chr2:113432691-113501204 |
| regionname0 | ZNG1B_chr2_113437691_113496204 |
| regionname5000 | ZNG1B_chr2_113432691_113501204 |
| 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 | 159 | 50 | 34 | 42 | 6 | 25 | 28 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002 | 0/0 | 395 | 94 | 12 | 22 | 48 | 3 | 9 | 29 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0003 | 0/0 | 395 | 20 | 20 | 0 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0004 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0005 | 0/0 | 395 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0006 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1188 | 154 | 48 | 34 | 42 | 6 | 22 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0002 | 0/0 | 1188 | 93 | 12 | 22 | 48 | 3 | 8 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0003 | 0/0 | 1188 | 20 | 20 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0004 | 0/0 | 1188 | 5 | 2 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0005 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0006 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0007 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| c0008 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 640 | 173 | 70 | 34 | 41 | 6 | 20 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0002 | 0/0 | 640 | 88 | 10 | 21 | 45 | 3 | 9 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0003 | 0/0 | 641 | 3 | 0 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0004 | 0/0 | 640 | 3 | 0 | 0 | 0 | 1 | 2 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0005 | 0/0 | 639 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0006 | 0/0 | 639 | 3 | 1 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0007 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0008 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| t0009 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0003 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1188 | 154 | 48 | 34 | 42 | 6 | 22 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0001c0004 | 0/0 | 1188 | 5 | 2 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002 | 0/0 | 1188 | 93 | 12 | 22 | 48 | 3 | 8 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0007 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0003c0003 | 0/0 | 1188 | 20 | 20 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0004c0006 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0005c0008 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0006c0005 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1827 | 150 | 48 | 34 | 41 | 5 | 20 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0001c0001t0004 | 0/0 | 1827 | 3 | 0 | 0 | 0 | 1 | 2 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0001c0001t0008 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0001c0004t0001 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0001c0004t0003 | 0/0 | 1828 | 3 | 0 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002t0002 | 0/0 | 1827 | 85 | 10 | 21 | 43 | 3 | 8 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002t0005 | 0/0 | 1826 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002t0006 | 0/0 | 1826 | 3 | 1 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002t0007 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0002t0009 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0002c0007t0002 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0003c0003t0001 | 0/0 | 1827 | 20 | 20 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0004c0006t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0005c0008t0001 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| a0006c0005t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | copy fasta | chr2 | 113432691 | 113501204 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0004c0006t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0005c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0006c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00140 | hp1 | a0005 | c0008 | t0001 | g0073 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0199 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00438 | hp2 | a0006 | c0005 | t0002 | g0002 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01069 | hp2 | a0002 | c0002 | t0007 | g0019 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0156 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0196 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0017 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0164 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0163 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0187 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0211 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0216 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0153 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0193 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0230 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02129 | hp2 | a0002 | c0002 | t0006 | g0206 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0225 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0172 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0238 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0241 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0237 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02965 | hp1 | a0002 | c0002 | t0009 | g0152 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0191 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0174 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0160 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0228 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0233 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0231 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0232 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0229 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0183 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03710 | hp2 | a0001 | c0004 | t0003 | g0227 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0210 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0180 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0022 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04184 | hp1 | a0002 | c0007 | t0002 | g0159 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0226 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0209 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | YRI | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18961 | hp2 | a0002 | c0002 | t0005 | g0189 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18964 | hp2 | a0002 | c0002 | t0006 | g0020 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18968 | hp2 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18982 | hp2 | a0004 | c0006 | t0002 | g0178 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19063 | hp2 | a0002 | c0002 | t0005 | g0213 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ASW | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0182 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0234 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA21309 | hp2 | a0002 | c0002 | t0006 | g0170 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0064 | REF | REF | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113443841
|
G | A | 1 | a0006 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.316G>A | p.Gly106Ser | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/15 | 494/1827 | 316/1188 | 106/395 | chr2 | 113443841 | ||
| chr2:113462485
|
C | T | 1 | a0005 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.653C>T | p.Ala218Val | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/15 | 831/1827 | 653/1188 | 218/395 | chr2 | 113462485 | ||
| chr2:113471049
|
G | A | 1 | a0003 | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
missense_variant | MODERATE | c.724G>A | p.Val242Ile | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/15 | 902/1827 | 724/1188 | 242/395 | chr2 | 113471049 | ||
| chr2:113495715
|
A | G | 3 | a0002a0004a0006 | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
missense_variant | MODERATE | c.1160A>G | p.His387Arg | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1338/1827 | 1160/1188 | 387/395 | chr2 | 113495715 | ||
| chr2:113495720
|
A | C | 2 | a0002a0006 | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
missense_variant | MODERATE | c.1165A>C | p.Lys389Gln | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1343/1827 | 1165/1188 | 389/395 | chr2 | 113495720 | ||
| chr2:113495724
|
A | C | 1 | a0004 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1169A>C | p.Glu390Ala | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1347/1827 | 1169/1188 | 390/395 | chr2 | 113495724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113462478
|
T | C | 6 | a0001c0004a0002c0002a0002c0007others(3): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
synonymous_variant | LOW | c.646T>C | p.Leu216Leu | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/15 | 824/1827 | 646/1188 | 216/395 | chr2 | 113462478 | ||
| chr2:113465153
|
C | T | 1 | a0002c0007 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.687C>T | p.Ile229Ile | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/15 | 865/1827 | 687/1188 | 229/395 | chr2 | 113465153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113437736
|
G | GA | 1 | a0001c0004t0003 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-132dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 131 | INFO_REALIGN_3_PRIME | chr2 | 113437736 | ||||
| chr2:113437766
|
A | C | 1 | a0002c0002t0009 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 103 | chr2 | 113437766 | |||||
| chr2:113437770
|
C | G | 1 | a0001c0004t0003 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-99C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 99 | chr2 | 113437770 | |||||
| chr2:113437781
|
C | T | 1 | a0001c0001t0008 | 1 | NA19002.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-88C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | chr2 | 113437781 | ||||||
| chr2:113437807
|
G | A | 1 | a0001c0001t0004 | 3 | HG01515.hp1 HG03710.hp1 HG03831.hp1 |
5_prime_UTR_variant | MODIFIER | c.-62G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 62 | chr2 | 113437807 | |||||
| chr2:113495803
|
A | G | 1 | a0002c0002t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 60 | chr2 | 113495803 | |||||
| chr2:113495894
|
G | A | 8 | a0002c0002t0002a0002c0002t0005a0002c0002t0006others(5): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 151 | chr2 | 113495894 | |||||
| chr2:113495970
|
G | A | 8 | a0002c0002t0002a0002c0002t0005a0002c0002t0006others(5): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 227 | chr2 | 113495970 | |||||
| chr2:113496051
|
AT | A | 1 | a0002c0002t0005 | 3 | NA18961.hp2 NA18968.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*314delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 314 | INFO_REALIGN_3_PRIME | chr2 | 113496051 | ||||
| chr2:113496058
|
C | T | 1 | a0002c0002t0007 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 315 | chr2 | 113496058 | |||||
| chr2:113496059
|
T | C | 1 | a0002c0002t0007 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 316 | chr2 | 113496059 | |||||
| chr2:113496107
|
AT | A | 1 | a0002c0002t0006 | 3 | HG02129.hp2 NA18964.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 371 | INFO_REALIGN_3_PRIME | chr2 | 113496107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113438232
|
T | C | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+210T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438232 | ||||||
| chr2:113438270
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 3 | HG01257.hp2 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.154+248T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438270 | ||||||
| chr2:113438348
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+326C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438348 | ||||||
| chr2:113438615
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+593G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438615 | ||||||
| chr2:113438696
|
C | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.154+674C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438696 | ||||||
| chr2:113438834
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+812C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438834 | ||||||
| chr2:113438850
|
T | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+828T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438850 | ||||||
| chr2:113438876
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+854C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438876 | ||||||
| chr2:113439157
|
A | C | 3 | a0003c0003t0001g0239a0003c0003t0001g0240a0003c0003t0001g0241 | 3 | HG02145.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.154+1135A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439157 | ||||||
| chr2:113439162
|
T | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.154+1140T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439162 | ||||||
| chr2:113439236
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+1214C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439236 | ||||||
| chr2:113439496
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.154+1474G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439496 | ||||||
| chr2:113439776
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.155-1575T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439776 | ||||||
| chr2:113439874
|
A | AT | 90 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 94 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.155-1449dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | |||||
| chr2:113439874
|
A | ATT | 38 | a0001c0001t0001g0031a0001c0001t0001g0131a0001c0001t0001g0132others(35): Show | 43 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.155-1450_155-1449d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | |||||
| chr2:113439874
|
A | ATTT | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0149others(7): Show | 10 | HG00735.hp2 HG01517.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-1451_155-1449d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | |||||
| chr2:113439874
|
AT | A | 22 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(19): Show | 25 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.155-1449delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | |||||
| chr2:113439874
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.155-1458_155-1449d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | |||||
| chr2:113439953
|
C | T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1398C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439953 | ||||||
| chr2:113439975
|
G | C | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.155-1376G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439975 | ||||||
| chr2:113440082
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.155-1269C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440082 | ||||||
| chr2:113440095
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.155-1256G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440095 | ||||||
| chr2:113440136
|
G | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.155-1215G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440136 | ||||||
| chr2:113440278
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.155-1073G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440278 | ||||||
| chr2:113440303
|
G | T | 64 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0019others(61): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.155-1048G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440303 | ||||||
| chr2:113440320
|
A | G | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1031A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440320 | ||||||
| chr2:113440348
|
C | G | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1003C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440348 | ||||||
| chr2:113440414
|
T | C | 1 | a0001c0004t0003g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.155-937T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440414 | ||||||
| chr2:113440467
|
C | G | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.155-884C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440467 | ||||||
| chr2:113440538
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.155-813C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440538 | ||||||
| chr2:113440559
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.155-792G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440559 | ||||||
| chr2:113440615
|
G | A | 1 | a0002c0002t0002g0153 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.155-736G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440615 | ||||||
| chr2:113440712
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.155-639C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440712 | ||||||
| chr2:113440893
|
G | T | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-458G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440893 | ||||||
| chr2:113441126
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0146others(2): Show | 5 | HG00099.hp2 HG00280.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-225A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441126 | ||||||
| chr2:113441142
|
G | C | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-209G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441142 | ||||||
| chr2:113441153
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.155-198T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441153 | ||||||
| chr2:113441319
|
ATTT | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-27_155-25delTT others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113441319 | |||||
| chr2:113441337
|
A | T | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-14A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441337 | ||||||
| chr2:113441942
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241+505G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113441942 | ||||||
| chr2:113441990
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+553G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113441990 | ||||||
| chr2:113442014
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.241+577C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442014 | ||||||
| chr2:113442197
|
C | T | 1 | a0002c0002t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.241+760C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442197 | ||||||
| chr2:113442265
|
AATATT | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.241+830_241+834del others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442265 | |||||
| chr2:113442349
|
G | A | 1 | a0003c0003t0001g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.241+912G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442349 | ||||||
| chr2:113442392
|
T | C | 13 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(10): Show | 15 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.241+955T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442392 | ||||||
| chr2:113442421
|
T | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.241+984T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442421 | ||||||
| chr2:113442561
|
TATC | T | 8 | a0002c0002t0002g0001a0002c0002t0002g0167a0002c0002t0002g0175others(5): Show | 11 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+1128_241+1130d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442561 | |||||
| chr2:113442696
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242-1071C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442696 | ||||||
| chr2:113442709
|
G | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.242-1058G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442709 | ||||||
| chr2:113442738
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.242-1029T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442738 | ||||||
| chr2:113442972
|
G | GT | 10 | a0001c0001t0004g0127a0001c0004t0001g0232a0001c0004t0001g0233others(7): Show | 12 | HG01361.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-781dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442972 | |||||
| chr2:113443015
|
C | A | 16 | a0003c0003t0001g0008a0003c0003t0001g0024a0003c0003t0001g0025others(13): Show | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.242-752C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443015 | ||||||
| chr2:113443067
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.242-700C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443067 | ||||||
| chr2:113443090
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.242-677G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443090 | ||||||
| chr2:113443211
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.242-556G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443211 | ||||||
| chr2:113443229
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.242-538G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443229 | ||||||
| chr2:113443457
|
G | A | 2 | a0002c0002t0002g0183a0002c0002t0002g0210 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.242-310G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443457 | ||||||
| chr2:113443594
|
C | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.242-173C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443594 | ||||||
| chr2:113443641
|
A | C | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-126A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443641 | ||||||
| chr2:113443880
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.338+17C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113443880 | ||||||
| chr2:113444118
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.338+255G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444118 | ||||||
| chr2:113444205
|
A | AG | 13 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0132others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+342_338+343ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444205 | ||||||
| chr2:113444523
|
A | G | 1 | a0002c0002t0002g0179 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.339-441A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444523 | ||||||
| chr2:113444783
|
A | G | 1 | a0002c0002t0002g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.339-181A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444783 | ||||||
| chr2:113444799
|
T | C | 1 | a0002c0002t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.339-165T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444799 | ||||||
| chr2:113444810
|
C | T | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-154C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444810 | ||||||
| chr2:113444859
|
AG | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.339-102delG | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 113444859 | |||||
| chr2:113445072
|
TTAA | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+21_430+23delTA others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445072 | |||||
| chr2:113445236
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430+181C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445236 | ||||||
| chr2:113445285
|
T | C | 1 | a0002c0002t0002g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.430+230T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445285 | ||||||
| chr2:113445300
|
T | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+245T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445300 | ||||||
| chr2:113445349
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430+294A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445349 | ||||||
| chr2:113445373
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.430+318G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445373 | ||||||
| chr2:113445398
|
T | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.430+343T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445398 | ||||||
| chr2:113445556
|
A | G | 5 | a0002c0002t0002g0215a0002c0002t0002g0216a0002c0002t0002g0217others(2): Show | 5 | HG00735.hp2 HG01099.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+501A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445556 | ||||||
| chr2:113445581
|
G | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.430+526G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445581 | ||||||
| chr2:113445596
|
G | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+541G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445596 | ||||||
| chr2:113445753
|
T | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+698T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445753 | ||||||
| chr2:113445763
|
TTCTGTGA others(1): Show |
T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.430+721_430+728del others(8): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445763 | |||||
| chr2:113445796
|
A | AT | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(36): Show | 44 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.430+758dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445796 | |||||
| chr2:113445796
|
AT | A | 67 | a0001c0001t0001g0028a0002c0002t0002g0001a0002c0002t0002g0002others(64): Show | 74 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.430+758delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445796 | |||||
| chr2:113445798
|
T | TA | 16 | a0003c0003t0001g0008a0003c0003t0001g0024a0003c0003t0001g0025others(13): Show | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+743_430+744ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445798 | ||||||
| chr2:113445799
|
T | A | 22 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0007others(19): Show | 25 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+744T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445799 | ||||||
| chr2:113445800
|
T | A | 65 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0019others(62): Show | 72 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.430+745T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445800 | ||||||
| chr2:113445801
|
T | A | 16 | a0003c0003t0001g0008a0003c0003t0001g0024a0003c0003t0001g0025others(13): Show | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+746T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445801 | ||||||
| chr2:113445802
|
T | A | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+747T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445802 | ||||||
| chr2:113445843
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.430+788G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445843 | ||||||
| chr2:113445844
|
T | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+789T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445844 | ||||||
| chr2:113445879
|
A | G | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0121others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+824A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445879 | ||||||
| chr2:113446212
|
C | T | 1 | a0003c0003t0001g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+1157C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446212 | ||||||
| chr2:113446237
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430+1182T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446237 | ||||||
| chr2:113446241
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430+1186G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446241 | ||||||
| chr2:113446289
|
A | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1234A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446289 | ||||||
| chr2:113446585
|
G | T | 2 | a0002c0002t0002g0174a0002c0002t0002g0208 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.430+1530G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446585 | ||||||
| chr2:113446645
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430+1590C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446645 | ||||||
| chr2:113446661
|
A | G | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+1606A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446661 | ||||||
| chr2:113446665
|
C | G | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+1610C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446665 | ||||||
| chr2:113446743
|
T | TAC | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1703_430+1704d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446743 | |||||
| chr2:113446765
|
T | C | 1 | a0002c0002t0002g0221 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.430+1710T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446765 | ||||||
| chr2:113446771
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0027a0002c0002t0002g0221 | 4 | HG01257.hp2 HG01258.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1716C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446771 | ||||||
| chr2:113446772
|
GCA | G | 19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0075others(16): Show | 19 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1736_430+1737d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | |||||
| chr2:113446772
|
GCACA | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1734_430+1737d others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | |||||
| chr2:113446772
|
GCACACA | G | 84 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(81): Show | 94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.430+1732_430+1737d others(8): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | |||||
| chr2:113446777
|
CACACACA others(13): Show |
C | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1736_430+1755d others(22): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446777 | |||||
| chr2:113446778
|
A | G | 1 | a0002c0002t0002g0221 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.430+1723A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446778 | ||||||
| chr2:113446838
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1783A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446838 | ||||||
| chr2:113446860
|
A | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1805A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446860 | ||||||
| chr2:113446958
|
C | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(23): Show | 27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+1903C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446958 | ||||||
| chr2:113447077
|
A | G | 1 | a0002c0002t0002g0166 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.430+2022A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447077 | ||||||
| chr2:113447106
|
A | G | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.430+2051A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447106 | ||||||
| chr2:113447154
|
G | T | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0121others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+2099G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447154 | ||||||
| chr2:113447283
|
T | TAAAAAAA others(3): Show |
6 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(3): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+2235_430+2244d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(4): Show |
11 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0024others(8): Show | 13 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+2234_430+2244d others(13): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(5): Show |
2 | a0002c0002t0002g0173a0003c0003t0001g0235 | 2 | HG01496.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.430+2233_430+2244d others(14): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(6): Show |
60 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0019others(57): Show | 67 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.430+2232_430+2244d others(15): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(7): Show |
18 | a0002c0002t0002g0007a0002c0002t0002g0018a0002c0002t0002g0157others(15): Show | 21 | HG00544.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+2231_430+2244d others(16): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(8): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0088a0002c0002t0002g0153others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+2230_430+2244d others(17): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(9): Show |
13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+2229_430+2244d others(18): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0095a0001c0001t0001g0142 | 3 | HG02895.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.430+2244_430+2245i others(19): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(11): Show |
15 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 16 | HG00639.hp1 HG00642.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(20): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(12): Show |
18 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0091others(15): Show | 18 | HG00099.hp2 HG01257.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(21): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(13): Show |
5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0111others(2): Show | 5 | HG00280.hp2 HG00639.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(22): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(14): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG01109.hp1 HG01517.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(23): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447283
|
T | TAAAAAAA others(15): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0131 | 2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.430+2244_430+2245i others(24): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | |||||
| chr2:113447413
|
T | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+2358T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447413 | ||||||
| chr2:113447711
|
T | C | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+2656T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447711 | ||||||
| chr2:113448070
|
T | C | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3015T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448070 | ||||||
| chr2:113448121
|
T | G | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+3066T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448121 | ||||||
| chr2:113448162
|
A | G | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+3107A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448162 | ||||||
| chr2:113448239
|
C | T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3184C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448239 | ||||||
| chr2:113448356
|
C | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3301C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448356 | ||||||
| chr2:113448574
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+3519A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448574 | ||||||
| chr2:113448627
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3572G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448627 | ||||||
| chr2:113448674
|
G | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+3619G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448674 | ||||||
| chr2:113448810
|
G | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+3755G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448810 | ||||||
| chr2:113448845
|
T | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.430+3790T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448845 | ||||||
| chr2:113448866
|
G | A | 16 | a0003c0003t0001g0008a0003c0003t0001g0024a0003c0003t0001g0025others(13): Show | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+3811G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448866 | ||||||
| chr2:113448874
|
G | T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3819G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448874 | ||||||
| chr2:113449036
|
T | C | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3981T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449036 | ||||||
| chr2:113449129
|
C | A | 2 | a0002c0002t0002g0167a0002c0002t0002g0175 | 2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.431-4010C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449129 | ||||||
| chr2:113449146
|
A | G | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-3993A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449146 | ||||||
| chr2:113449351
|
G | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-3788G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449351 | ||||||
| chr2:113449381
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-3758C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449381 | ||||||
| chr2:113449547
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-3592A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449547 | ||||||
| chr2:113449565
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-3574T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449565 | ||||||
| chr2:113449582
|
C | T | 1 | a0005c0008t0001g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.431-3557C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449582 | ||||||
| chr2:113449829
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-3310T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449829 | ||||||
| chr2:113449938
|
G | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-3201G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449938 | ||||||
| chr2:113450048
|
A | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-3091A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450048 | ||||||
| chr2:113450269
|
G | A | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(114): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-2870G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450269 | ||||||
| chr2:113450351
|
C | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-2788C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450351 | ||||||
| chr2:113450363
|
G | A | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-2776G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450363 | ||||||
| chr2:113450581
|
G | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.431-2558G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450581 | ||||||
| chr2:113450686
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-2453G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450686 | ||||||
| chr2:113451248
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-1891G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451248 | ||||||
| chr2:113451255
|
G | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-1884G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451255 | ||||||
| chr2:113451575
|
T | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-1564T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451575 | ||||||
| chr2:113451925
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-1214T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451925 | ||||||
| chr2:113452068
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0142 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.431-1071G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452068 | ||||||
| chr2:113452406
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0137 | 2 | HG00642.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.431-733C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452406 | ||||||
| chr2:113452443
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-696C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452443 | ||||||
| chr2:113452790
|
C | A | 166 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(163): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.431-349C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452790 | ||||||
| chr2:113453240
|
GT | G | 100 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(97): Show | 114 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.490+53delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453240 | |||||
| chr2:113453241
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490+43T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453241 | ||||||
| chr2:113453247
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490+49T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453247 | ||||||
| chr2:113453251
|
T | A | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+53T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453251 | ||||||
| chr2:113453344
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.490+146C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453344 | ||||||
| chr2:113453418
|
A | T | 51 | a0002c0002t0002g0002a0002c0002t0002g0019a0002c0002t0002g0020others(48): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+220A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453418 | ||||||
| chr2:113453489
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.490+291G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453489 | ||||||
| chr2:113453504
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490+306C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453504 | ||||||
| chr2:113453532
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490+334C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453532 | ||||||
| chr2:113453698
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.490+500T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453698 | ||||||
| chr2:113453754
|
T | TA | 89 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227others(86): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.490+566dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453754 | |||||
| chr2:113453754
|
T | TAA | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.490+565_490+566dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453754 | |||||
| chr2:113453843
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.490+645C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453843 | ||||||
| chr2:113453854
|
G | T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+656G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453854 | ||||||
| chr2:113454321
|
A | G | 1 | a0002c0002t0002g0166 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.491-420A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454321 | ||||||
| chr2:113454331
|
T | A | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.491-410T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454331 | ||||||
| chr2:113454455
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.491-286G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454455 | ||||||
| chr2:113454553
|
G | A | 18 | a0002c0002t0002g0007a0002c0002t0002g0018a0002c0002t0002g0153others(15): Show | 21 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.491-188G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454553 | ||||||
| chr2:113454573
|
T | C | 1 | a0002c0002t0002g0188 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.491-168T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454573 | ||||||
| chr2:113454882
|
A | G | 10 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.528+104A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113454882 | ||||||
| chr2:113454970
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.528+192C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113454970 | ||||||
| chr2:113455094
|
T | C | 1 | a0002c0002t0002g0153 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.528+316T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455094 | ||||||
| chr2:113455180
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(15): Show | 19 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.528+402T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455180 | ||||||
| chr2:113455242
|
G | A | 1 | a0002c0002t0002g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.528+464G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455242 | ||||||
| chr2:113455251
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+473T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455251 | ||||||
| chr2:113455291
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.528+513T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455291 | ||||||
| chr2:113455368
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.528+590G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455368 | ||||||
| chr2:113455466
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0138 | 3 | HG02257.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.528+688T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455466 | ||||||
| chr2:113455722
|
AT | A | 87 | a0001c0001t0001g0042a0002c0002t0002g0001a0002c0002t0002g0002others(84): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.528+960delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113455722 | |||||
| chr2:113455852
|
C | CTG | 121 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(118): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.528+1074_528+1075i others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455852 | ||||||
| chr2:113455970
|
G | A | 2 | a0002c0002t0002g0187a0002c0002t0009g0152 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.528+1192G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455970 | ||||||
| chr2:113456140
|
C | T | 2 | a0002c0002t0002g0020a0002c0002t0006g0020 | 2 | NA18944.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.528+1362C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456140 | ||||||
| chr2:113456273
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.528+1495G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456273 | ||||||
| chr2:113456454
|
G | GT | 14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(11): Show | 14 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.528+1687dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113456454 | |||||
| chr2:113456454
|
GTT | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+1686_528+1687d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113456454 | |||||
| chr2:113456748
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.528+1970C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456748 | ||||||
| chr2:113457299
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.528+2521A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457299 | ||||||
| chr2:113457603
|
A | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.528+2825A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457603 | ||||||
| chr2:113457652
|
A | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.528+2874A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457652 | ||||||
| chr2:113457715
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+2937T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457715 | ||||||
| chr2:113457760
|
G | GA | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2913_529-2912i others(3): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457760 | ||||||
| chr2:113457908
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.529-2765G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457908 | ||||||
| chr2:113458154
|
A | T | 3 | a0002c0002t0002g0007a0002c0002t0002g0163a0002c0002t0002g0164 | 5 | HG01192.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-2519A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458154 | ||||||
| chr2:113458302
|
A | G | 2 | a0002c0002t0002g0181a0002c0002t0002g0182 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-2371A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458302 | ||||||
| chr2:113458351
|
A | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2322A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458351 | ||||||
| chr2:113458363
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.529-2310A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458363 | ||||||
| chr2:113458385
|
G | C | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.529-2288G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458385 | ||||||
| chr2:113458385
|
G | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.529-2288G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458385 | ||||||
| chr2:113458386
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.529-2287G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458386 | ||||||
| chr2:113458405
|
A | C | 2 | a0002c0002t0002g0153a0002c0002t0002g0156 | 2 | HG01167.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.529-2268A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458405 | ||||||
| chr2:113458576
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2097A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458576 | ||||||
| chr2:113458728
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.529-1945C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458728 | ||||||
| chr2:113458932
|
C | A | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1741C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458932 | ||||||
| chr2:113459099
|
A | T | 2 | a0002c0002t0002g0163a0002c0002t0002g0164 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1574A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459099 | ||||||
| chr2:113459403
|
T | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-1270T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459403 | ||||||
| chr2:113459542
|
TA | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.529-1121delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113459542 | |||||
| chr2:113459817
|
G | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-856G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459817 | ||||||
| chr2:113459899
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.529-774G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459899 | ||||||
| chr2:113459903
|
GA | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.529-760delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113459903 | |||||
| chr2:113459904
|
A | G | 10 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-769A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459904 | ||||||
| chr2:113460238
|
T | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.529-435T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113460238 | ||||||
| chr2:113460489
|
T | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.529-184T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113460489 | ||||||
| chr2:113460733
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.575+14A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460733 | ||||||
| chr2:113460734
|
A | C | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.575+15A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460734 | ||||||
| chr2:113460768
|
A | G | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.575+49A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460768 | ||||||
| chr2:113460933
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.575+214G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460933 | ||||||
| chr2:113461027
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.575+308T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461027 | ||||||
| chr2:113461027
|
T | TTA | 84 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0098others(81): Show | 94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.575+324_575+325dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461027 | |||||
| chr2:113461027
|
T | TTATATAT others(3): Show |
1 | a0001c0004t0001g0232 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.575+316_575+325dup others(10): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461027 | |||||
| chr2:113461058
|
A | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.575+339A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461058 | ||||||
| chr2:113461061
|
T | A | 20 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0044others(17): Show | 23 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.575+342T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461061 | ||||||
| chr2:113461228
|
T | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.575+509T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461228 | ||||||
| chr2:113461228
|
T | C | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.575+509T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461228 | ||||||
| chr2:113461229
|
T | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.575+510T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461229 | ||||||
| chr2:113461230
|
T | A | 96 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227others(93): Show | 108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.575+511T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461230 | ||||||
| chr2:113461263
|
G | A | 4 | a0002c0002t0002g0007a0002c0002t0002g0018a0002c0002t0002g0163others(1): Show | 7 | HG01192.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+544G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461263 | ||||||
| chr2:113461328
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.575+609C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461328 | ||||||
| chr2:113461467
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.575+748G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461467 | ||||||
| chr2:113461586
|
GA | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576-818delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461586 | |||||
| chr2:113461607
|
T | A | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.576-801T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461607 | ||||||
| chr2:113461839
|
T | G | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.576-569T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461839 | ||||||
| chr2:113462086
|
T | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.576-322T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462086 | ||||||
| chr2:113462136
|
G | A | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.576-272G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462136 | ||||||
| chr2:113462228
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.576-180C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462228 | ||||||
| chr2:113462229
|
G | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.576-179G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462229 | ||||||
| chr2:113462359
|
C | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.576-49C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462359 | ||||||
| chr2:113462540
|
T | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.662+46T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462540 | ||||||
| chr2:113462782
|
A | G | 2 | a0001c0001t0001g0095a0002c0002t0009g0152 | 2 | HG02965.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.662+288A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462782 | ||||||
| chr2:113462901
|
GT | G | 47 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(44): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.662+425delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | |||||
| chr2:113462901
|
GTT | G | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(87): Show | 98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.662+424_662+425del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | |||||
| chr2:113462901
|
GTTT | G | 11 | a0002c0002t0002g0021a0002c0002t0002g0192a0003c0003t0001g0008others(8): Show | 14 | HG01943.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.662+423_662+425del others(3): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | |||||
| chr2:113462919
|
T | A | 1 | a0002c0002t0002g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.662+425T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462919 | ||||||
| chr2:113462933
|
C | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.662+439C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462933 | ||||||
| chr2:113462954
|
C | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.662+460C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462954 | ||||||
| chr2:113463127
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+633C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463127 | ||||||
| chr2:113463335
|
G | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.662+841G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463335 | ||||||
| chr2:113463474
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.662+980A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463474 | ||||||
| chr2:113463535
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+1041G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463535 | ||||||
| chr2:113463786
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.662+1292A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463786 | ||||||
| chr2:113464501
|
G | GAAAAGAA others(306): Show |
1 | a0002c0002t0002g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-609_663-608ins others(313): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | |||||
| chr2:113464501
|
G | GAAAAGAA others(309): Show |
2 | a0002c0002t0002g0173a0004c0006t0002g0178 | 2 | HG01496.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.663-609_663-608ins others(316): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | |||||
| chr2:113464501
|
G | GAAAAGAA others(310): Show |
77 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(74): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.663-609_663-608ins others(317): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | |||||
| chr2:113464501
|
G | GAAAAGAA others(311): Show |
5 | a0002c0002t0002g0204a0002c0002t0002g0207a0002c0002t0006g0170others(2): Show | 5 | HG02074.hp2 HG02965.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-609_663-608ins others(318): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | |||||
| chr2:113464501
|
G | GAAAAGAA others(311): Show |
1 | a0002c0002t0002g0212 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.663-609_663-608ins others(318): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | |||||
| chr2:113464719
|
A | G | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.663-410A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464719 | ||||||
| chr2:113464832
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0150 | 2 | HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.663-297C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464832 | ||||||
| chr2:113464843
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.663-286C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464843 | ||||||
| chr2:113465056
|
T | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.663-73T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113465056 | ||||||
| chr2:113465249
|
T | G | 1 | a0002c0002t0005g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.707+76T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465249 | ||||||
| chr2:113465325
|
T | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+152T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465325 | ||||||
| chr2:113465381
|
A | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+208A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465381 | ||||||
| chr2:113465504
|
G | GT | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.707+334dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465504 | |||||
| chr2:113465744
|
A | AT | 75 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0044others(72): Show | 84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.707+597dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | |||||
| chr2:113465744
|
A | ATT | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0105others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.707+596_707+597dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | |||||
| chr2:113465744
|
AT | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 65 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.707+597delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | |||||
| chr2:113465744
|
ATT | A | 9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(6): Show | 9 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+596_707+597del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | |||||
| chr2:113465744
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.707+586_707+597del others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | |||||
| chr2:113465820
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.707+647C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465820 | ||||||
| chr2:113465899
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.707+726C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465899 | ||||||
| chr2:113466050
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.707+877G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466050 | ||||||
| chr2:113466082
|
A | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+909A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466082 | ||||||
| chr2:113466103
|
A | C | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707+930A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466103 | ||||||
| chr2:113466327
|
G | A | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+1154G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466327 | ||||||
| chr2:113466549
|
TTCC | T | 64 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0019others(61): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.707+1377_707+1379d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466549 | ||||||
| chr2:113466552
|
C | T | 43 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(40): Show | 50 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.707+1379C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466552 | ||||||
| chr2:113466636
|
T | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+1463T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466636 | ||||||
| chr2:113466793
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.707+1620G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466793 | ||||||
| chr2:113466901
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.707+1728A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466901 | ||||||
| chr2:113466980
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.707+1807C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466980 | ||||||
| chr2:113466981
|
G | A | 1 | a0002c0002t0002g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.707+1808G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466981 | ||||||
| chr2:113467025
|
C | T | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+1852C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467025 | ||||||
| chr2:113467063
|
C | CA | 28 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(25): Show | 30 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.707+1905dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113467063 | |||||
| chr2:113467063
|
C | CAA | 6 | a0001c0001t0001g0129a0003c0003t0001g0026a0003c0003t0001g0234others(3): Show | 6 | HG01175.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+1904_707+1905d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113467063 | |||||
| chr2:113467079
|
C | A | 19 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0181others(16): Show | 23 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.707+1906C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467079 | ||||||
| chr2:113467162
|
A | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.707+1989A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467162 | ||||||
| chr2:113467357
|
A | T | 1 | a0002c0002t0002g0155 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.707+2184A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467357 | ||||||
| chr2:113467678
|
C | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+2505C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467678 | ||||||
| chr2:113467884
|
A | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+2711A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467884 | ||||||
| chr2:113467911
|
C | G | 2 | a0002c0002t0002g0153a0002c0002t0002g0156 | 2 | HG01167.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.707+2738C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467911 | ||||||
| chr2:113467968
|
A | G | 1 | a0002c0002t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.707+2795A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467968 | ||||||
| chr2:113468121
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0138 | 3 | HG02257.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.708-2912G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468121 | ||||||
| chr2:113468157
|
G | A | 1 | a0002c0002t0002g0018 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.708-2876G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468157 | ||||||
| chr2:113468175
|
T | A | 1 | a0001c0001t0001g0054 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.708-2858T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468175 | ||||||
| chr2:113468201
|
T | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-2832T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468201 | ||||||
| chr2:113468238
|
G | T | 1 | a0002c0002t0006g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.708-2795G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468238 | ||||||
| chr2:113468455
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0114a0001c0001t0001g0119others(2): Show | 5 | HG02559.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-2578A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468455 | ||||||
| chr2:113468483
|
G | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.708-2550G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468483 | ||||||
| chr2:113468615
|
C | CT | 21 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(18): Show | 25 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.708-2406dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113468615 | |||||
| chr2:113468786
|
C | G | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.708-2247C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468786 | ||||||
| chr2:113469041
|
T | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 65 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.708-1992T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469041 | ||||||
| chr2:113469206
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.708-1827C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469206 | ||||||
| chr2:113469269
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.708-1764G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469269 | ||||||
| chr2:113469349
|
C | T | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.708-1684C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469349 | ||||||
| chr2:113469458
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(110): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.708-1575A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469458 | ||||||
| chr2:113469667
|
T | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-1366T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469667 | ||||||
| chr2:113469980
|
C | T | 1 | a0002c0002t0002g0018 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.708-1053C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469980 | ||||||
| chr2:113469991
|
C | CT | 103 | a0001c0001t0001g0148a0001c0004t0001g0232a0001c0004t0001g0233others(100): Show | 116 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.708-1027dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113469991 | |||||
| chr2:113470016
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG02523.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.708-1017C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470016 | ||||||
| chr2:113470107
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.708-926G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470107 | ||||||
| chr2:113470127
|
G | C | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0227others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.708-906G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470127 | ||||||
| chr2:113470139
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.708-894G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470139 | ||||||
| chr2:113470273
|
C | G | 2 | a0001c0004t0003g0225a0001c0004t0003g0226 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.708-760C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470273 | ||||||
| chr2:113470515
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.708-518T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470515 | ||||||
| chr2:113470549
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.708-484C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470549 | ||||||
| chr2:113470692
|
T | A | 2 | a0002c0002t0002g0194a0002c0002t0002g0201 | 2 | HG00673.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.708-341T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470692 | ||||||
| chr2:113470706
|
A | C | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.708-327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470706 | ||||||
| chr2:113470847
|
A | G | 1 | a0002c0002t0002g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.708-186A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470847 | ||||||
| chr2:113471292
|
A | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+203A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471292 | ||||||
| chr2:113471327
|
G | A | 99 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(96): Show | 109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.764+238G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471327 | ||||||
| chr2:113471416
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0044 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.764+327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471416 | ||||||
| chr2:113471466
|
GT | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+386delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113471466 | |||||
| chr2:113471480
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+391T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471480 | ||||||
| chr2:113471553
|
A | G | 1 | a0002c0002t0002g0154 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.764+464A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471553 | ||||||
| chr2:113471572
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.764+483G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471572 | ||||||
| chr2:113471631
|
C | G | 1 | a0002c0002t0006g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.764+542C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471631 | ||||||
| chr2:113471651
|
G | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+562G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471651 | ||||||
| chr2:113471761
|
T | C | 138 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(135): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.764+672T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471761 | ||||||
| chr2:113471795
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.764+706C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471795 | ||||||
| chr2:113471940
|
CAT | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+854_764+855del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113471940 | |||||
| chr2:113471955
|
G | A | 1 | a0002c0002t0002g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.764+866G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471955 | ||||||
| chr2:113472036
|
G | C | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+947G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472036 | ||||||
| chr2:113472054
|
G | A | 2 | a0002c0002t0002g0167a0002c0002t0002g0175 | 2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.764+965G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472054 | ||||||
| chr2:113472073
|
T | C | 1 | a0002c0002t0002g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.764+984T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472073 | ||||||
| chr2:113472093
|
T | C | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+1004T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472093 | ||||||
| chr2:113472096
|
G | A | 16 | a0003c0003t0001g0008a0003c0003t0001g0024a0003c0003t0001g0025others(13): Show | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.764+1007G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472096 | ||||||
| chr2:113472176
|
C | G | 1 | a0001c0001t0001g0012 | 2 | NA18979.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.764+1087C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472176 | ||||||
| chr2:113472192
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1103A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472192 | ||||||
| chr2:113472304
|
G | A | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.764+1215G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472304 | ||||||
| chr2:113472347
|
G | A | 1 | a0002c0002t0002g0196 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.764+1258G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472347 | ||||||
| chr2:113472409
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1320C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472409 | ||||||
| chr2:113472424
|
A | G | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1335A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472424 | ||||||
| chr2:113472428
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.764+1339T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472428 | ||||||
| chr2:113472445
|
C | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1356C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472445 | ||||||
| chr2:113472445
|
C | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.764+1356C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472445 | ||||||
| chr2:113472592
|
C | T | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+1503C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472592 | ||||||
| chr2:113472684
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1595G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472684 | ||||||
| chr2:113472801
|
T | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1712T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472801 | ||||||
| chr2:113472837
|
G | T | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+1748G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472837 | ||||||
| chr2:113472838
|
A | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+1749A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472838 | ||||||
| chr2:113472900
|
A | T | 2 | a0002c0002t0002g0161a0002c0002t0002g0165 | 2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.764+1811A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472900 | ||||||
| chr2:113472987
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1898A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472987 | ||||||
| chr2:113473093
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.764+2004C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473093 | ||||||
| chr2:113473190
|
G | A | 1 | a0002c0002t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.764+2101G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473190 | ||||||
| chr2:113473325
|
T | C | 1 | a0002c0002t0002g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.764+2236T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473325 | ||||||
| chr2:113473389
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.764+2300G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473389 | ||||||
| chr2:113473414
|
T | C | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+2325T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473414 | ||||||
| chr2:113473445
|
G | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2356G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473445 | ||||||
| chr2:113473466
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2377A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473466 | ||||||
| chr2:113473490
|
C | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+2401C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473490 | ||||||
| chr2:113473515
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2426A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473515 | ||||||
| chr2:113473696
|
T | C | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+2607T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473696 | ||||||
| chr2:113473779
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.764+2690T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473779 | ||||||
| chr2:113473781
|
G | C | 1 | a0001c0004t0003g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.764+2692G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473781 | ||||||
| chr2:113473821
|
G | A | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+2732G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473821 | ||||||
| chr2:113473835
|
G | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.764+2746G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473835 | ||||||
| chr2:113473858
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.764+2769G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473858 | ||||||
| chr2:113473881
|
C | T | 88 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227others(85): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.764+2792C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473881 | ||||||
| chr2:113473899
|
C | T | 108 | a0001c0001t0001g0051a0001c0004t0001g0232a0001c0004t0001g0233others(105): Show | 122 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.764+2810C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473899 | ||||||
| chr2:113473917
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.764+2828A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473917 | ||||||
| chr2:113474034
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764+2945A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474034 | ||||||
| chr2:113474061
|
C | G | 2 | a0001c0001t0001g0039a0002c0002t0002g0173 | 2 | HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+2972C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474061 | ||||||
| chr2:113474263
|
G | A | 1 | a0002c0002t0002g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+3174G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474263 | ||||||
| chr2:113474267
|
A | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+3178A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474267 | ||||||
| chr2:113474272
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.764+3183C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474272 | ||||||
| chr2:113474356
|
C | T | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.764+3267C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474356 | ||||||
| chr2:113474359
|
C | T | 1 | a0002c0002t0002g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.764+3270C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474359 | ||||||
| chr2:113474403
|
G | A | 1 | a0002c0002t0002g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.764+3314G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474403 | ||||||
| chr2:113474474
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.764+3385G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474474 | ||||||
| chr2:113474599
|
C | T | 13 | a0002c0002t0002g0023a0002c0002t0002g0183a0002c0002t0002g0186others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.764+3510C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474599 | ||||||
| chr2:113474613
|
G | C | 166 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(163): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.764+3524G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474613 | ||||||
| chr2:113474647
|
T | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(36): Show | 40 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.764+3558T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474647 | ||||||
| chr2:113474663
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.764+3574C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474663 | ||||||
| chr2:113474676
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+3587C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474676 | ||||||
| chr2:113474753
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.764+3664A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474753 | ||||||
| chr2:113474765
|
G | A | 4 | a0002c0002t0002g0007a0002c0002t0002g0018a0002c0002t0002g0163others(1): Show | 7 | HG01192.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.764+3676G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474765 | ||||||
| chr2:113474909
|
G | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+3820G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474909 | ||||||
| chr2:113475118
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.764+4029G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475118 | ||||||
| chr2:113475202
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764+4113G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475202 | ||||||
| chr2:113475234
|
C | T | 1 | a0002c0002t0002g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+4145C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475234 | ||||||
| chr2:113475364
|
A | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+4275A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475364 | ||||||
| chr2:113475371
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+4282G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475371 | ||||||
| chr2:113475381
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.764+4292G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475381 | ||||||
| chr2:113475406
|
T | C | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+4317T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475406 | ||||||
| chr2:113475412
|
C | T | 1 | a0002c0002t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.764+4323C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475412 | ||||||
| chr2:113475445
|
T | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4356T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475445 | ||||||
| chr2:113475459
|
T | C | 1 | a0002c0002t0002g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+4370T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475459 | ||||||
| chr2:113475509
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+4420C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475509 | ||||||
| chr2:113475592
|
C | A | 1 | a0002c0002t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.764+4503C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475592 | ||||||
| chr2:113475597
|
C | T | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+4508C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475597 | ||||||
| chr2:113475618
|
T | C | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+4529T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475618 | ||||||
| chr2:113475720
|
A | G | 1 | a0002c0002t0002g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.764+4631A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475720 | ||||||
| chr2:113475773
|
T | A | 3 | a0003c0003t0001g0239a0003c0003t0001g0240a0003c0003t0001g0241 | 3 | HG02145.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.764+4684T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475773 | ||||||
| chr2:113475782
|
G | A | 1 | a0002c0002t0002g0212 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.764+4693G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475782 | ||||||
| chr2:113475816
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4727C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475816 | ||||||
| chr2:113475861
|
T | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4772T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475861 | ||||||
| chr2:113476028
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+4939C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476028 | ||||||
| chr2:113476278
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.764+5189G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476278 | ||||||
| chr2:113476318
|
T | C | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+5229T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476318 | ||||||
| chr2:113476448
|
G | C | 1 | a0002c0002t0002g0216 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.764+5359G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476448 | ||||||
| chr2:113476490
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0094 | 5 | HG02622.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.764+5401C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476490 | ||||||
| chr2:113476532
|
A | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+5443A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476532 | ||||||
| chr2:113476535
|
AGCTGCGT others(20): Show |
A | 1 | a0002c0002t0002g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.764+5459_764+5485d others(29): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113476535 | |||||
| chr2:113476548
|
C | T | 120 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(117): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.764+5459C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476548 | ||||||
| chr2:113476552
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.764+5463G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476552 | ||||||
| chr2:113476688
|
C | G | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.765-5489C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476688 | ||||||
| chr2:113476688
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.765-5489C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476688 | ||||||
| chr2:113476713
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.765-5464T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476713 | ||||||
| chr2:113476848
|
T | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.765-5329T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476848 | ||||||
| chr2:113477105
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-5072C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477105 | ||||||
| chr2:113477180
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.765-4997C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477180 | ||||||
| chr2:113477181
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-4996G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477181 | ||||||
| chr2:113477186
|
A | AC | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 3 | HG01257.hp2 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.765-4988dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113477186 | |||||
| chr2:113477242
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.765-4935C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477242 | ||||||
| chr2:113477251
|
G | A | 1 | a0002c0002t0005g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.765-4926G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477251 | ||||||
| chr2:113477278
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-4899C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477278 | ||||||
| chr2:113477284
|
G | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4893G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477284 | ||||||
| chr2:113477327
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-4850C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477327 | ||||||
| chr2:113477340
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081 | 3 | HG00280.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.765-4837G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477340 | ||||||
| chr2:113477363
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4814C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477363 | ||||||
| chr2:113477379
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(12): Show | 16 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.765-4798G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477379 | ||||||
| chr2:113477408
|
G | A | 1 | a0002c0007t0002g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.765-4769G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477408 | ||||||
| chr2:113477442
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-4735C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477442 | ||||||
| chr2:113477897
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.765-4280G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477897 | ||||||
| chr2:113477901
|
G | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4276G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477901 | ||||||
| chr2:113477911
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4266G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477911 | ||||||
| chr2:113477991
|
A | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4186A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477991 | ||||||
| chr2:113477993
|
T | G | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.765-4184T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477993 | ||||||
| chr2:113478289
|
A | AT | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-3881dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478289 | |||||
| chr2:113478377
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-3800G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478377 | ||||||
| chr2:113478423
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.765-3754G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478423 | ||||||
| chr2:113478644
|
G | GT | 102 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227others(99): Show | 116 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.765-3522dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478644 | |||||
| chr2:113478789
|
T | TA | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0034others(4): Show | 11 | HG01952.hp2 HG02040.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-3378dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478789 | |||||
| chr2:113478866
|
G | A | 19 | a0001c0001t0001g0115a0001c0004t0001g0232a0001c0004t0001g0233others(16): Show | 23 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.765-3311G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478866 | ||||||
| chr2:113478926
|
T | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.765-3251T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478926 | ||||||
| chr2:113478978
|
G | A | 1 | a0002c0002t0002g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.765-3199G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478978 | ||||||
| chr2:113479036
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.765-3141G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479036 | ||||||
| chr2:113479191
|
C | A | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.765-2986C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479191 | ||||||
| chr2:113479344
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.765-2833A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479344 | ||||||
| chr2:113479347
|
T | C | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-2830T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479347 | ||||||
| chr2:113479461
|
C | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(23): Show | 27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.765-2716C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479461 | ||||||
| chr2:113479812
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.765-2365C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479812 | ||||||
| chr2:113479832
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.765-2345T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479832 | ||||||
| chr2:113479871
|
G | C | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-2306G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479871 | ||||||
| chr2:113479930
|
T | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-2247T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479930 | ||||||
| chr2:113480021
|
A | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-2156A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480021 | ||||||
| chr2:113480052
|
C | T | 1 | a0003c0003t0001g0237 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.765-2125C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480052 | ||||||
| chr2:113480223
|
C | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-1954C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480223 | ||||||
| chr2:113480406
|
A | C | 10 | a0001c0001t0001g0097a0003c0003t0001g0024a0003c0003t0001g0025others(7): Show | 12 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.765-1771A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480406 | ||||||
| chr2:113480574
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-1603C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480574 | ||||||
| chr2:113480915
|
A | G | 1 | a0002c0002t0002g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.765-1262A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480915 | ||||||
| chr2:113480948
|
C | T | 4 | a0002c0002t0002g0186a0002c0002t0002g0207a0002c0002t0002g0223others(1): Show | 4 | HG02056.hp1 HG02074.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-1229C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480948 | ||||||
| chr2:113481085
|
AT | A | 5 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227others(2): Show | 5 | HG01978.hp2 HG02698.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-1072delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | |||||
| chr2:113481085
|
ATT | A | 77 | a0001c0001t0001g0097a0002c0002t0002g0001a0002c0002t0002g0002others(74): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.765-1073_765-1072d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | |||||
| chr2:113481085
|
ATTT | A | 26 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0007others(23): Show | 31 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.765-1074_765-1072d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | |||||
| chr2:113481110
|
C | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-1067C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481110 | ||||||
| chr2:113481139
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | HG01099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.765-1038A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481139 | ||||||
| chr2:113481181
|
T | TC | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-995dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481181 | |||||
| chr2:113481299
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.765-878A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481299 | ||||||
| chr2:113481325
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.765-852C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481325 | ||||||
| chr2:113481344
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.765-833C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481344 | ||||||
| chr2:113481353
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.765-824C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481353 | ||||||
| chr2:113481397
|
C | T | 91 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0097others(88): Show | 102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.765-780C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481397 | ||||||
| chr2:113481636
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-541C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481636 | ||||||
| chr2:113481666
|
A | G | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.765-511A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481666 | ||||||
| chr2:113481674
|
A | G | 1 | a0003c0003t0001g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.765-503A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481674 | ||||||
| chr2:113481714
|
A | G | 1 | a0002c0002t0002g0205 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.765-463A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481714 | ||||||
| chr2:113481757
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-420C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481757 | ||||||
| chr2:113481955
|
G | A | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-222G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481955 | ||||||
| chr2:113481976
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.765-201T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481976 | ||||||
| chr2:113482007
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-170C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482007 | ||||||
| chr2:113482035
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-142G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482035 | ||||||
| chr2:113482119
|
C | T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-58C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482119 | ||||||
| chr2:113482147
|
A | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-30A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482147 | ||||||
| chr2:113482391
|
GTCTAAT | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+168_816+173del others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113482391 | |||||
| chr2:113482693
|
A | C | 1 | a0001c0001t0001g0051 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.816+465A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482693 | ||||||
| chr2:113482763
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816+535G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482763 | ||||||
| chr2:113482781
|
A | G | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+553A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482781 | ||||||
| chr2:113482944
|
C | CT | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+717dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113482944 | |||||
| chr2:113483151
|
T | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+923T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483151 | ||||||
| chr2:113483241
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0106 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.816+1013C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483241 | ||||||
| chr2:113483276
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+1048T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483276 | ||||||
| chr2:113483315
|
G | A | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+1087G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483315 | ||||||
| chr2:113483510
|
C | T | 4 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(1): Show | 6 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+1282C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483510 | ||||||
| chr2:113483565
|
A | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+1337A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483565 | ||||||
| chr2:113483735
|
A | T | 64 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0019others(61): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.816+1507A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483735 | ||||||
| chr2:113483747
|
T | A | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.816+1519T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483747 | ||||||
| chr2:113484023
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+1795G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484023 | ||||||
| chr2:113484289
|
C | A | 1 | a0002c0002t0002g0177 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.816+2061C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484289 | ||||||
| chr2:113484294
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.816+2066A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484294 | ||||||
| chr2:113484619
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.816+2391G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484619 | ||||||
| chr2:113484648
|
G | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(15): Show | 19 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+2420G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484648 | ||||||
| chr2:113484663
|
G | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+2435G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484663 | ||||||
| chr2:113484811
|
T | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0038others(23): Show | 27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.816+2583T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484811 | ||||||
| chr2:113484837
|
AT | A | 10 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0090others(7): Show | 10 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+2625delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113484837 | |||||
| chr2:113484954
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.816+2726T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484954 | ||||||
| chr2:113485174
|
C | T | 1 | a0002c0002t0002g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.816+2946C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485174 | ||||||
| chr2:113485193
|
C | G | 166 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(163): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.816+2965C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485193 | ||||||
| chr2:113485337
|
A | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+3109A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485337 | ||||||
| chr2:113485552
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+3324G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485552 | ||||||
| chr2:113485571
|
G | A | 3 | a0002c0002t0002g0171a0002c0002t0002g0174a0002c0002t0002g0208 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+3343G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485571 | ||||||
| chr2:113485880
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0142 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.816+3652G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485880 | ||||||
| chr2:113485982
|
G | A | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+3754G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485982 | ||||||
| chr2:113486008
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.816+3780A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486008 | ||||||
| chr2:113486024
|
A | C | 4 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(1): Show | 6 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+3796A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486024 | ||||||
| chr2:113486283
|
G | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+4055G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486283 | ||||||
| chr2:113486442
|
T | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.816+4214T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486442 | ||||||
| chr2:113486505
|
A | G | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+4277A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486505 | ||||||
| chr2:113486551
|
T | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0121others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.816+4323T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486551 | ||||||
| chr2:113486746
|
A | AC | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+4522dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113486746 | |||||
| chr2:113486805
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+4577G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486805 | ||||||
| chr2:113486813
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.816+4585C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486813 | ||||||
| chr2:113486890
|
T | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0114a0001c0001t0001g0119others(2): Show | 5 | HG02559.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+4662T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486890 | ||||||
| chr2:113486901
|
T | C | 1 | a0002c0002t0002g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.816+4673T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486901 | ||||||
| chr2:113486919
|
C | T | 1 | a0002c0002t0002g0223 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.816+4691C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486919 | ||||||
| chr2:113487001
|
AG | A | 121 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0079others(118): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.816+4774delG | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487001 | ||||||
| chr2:113487217
|
G | A | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+4989G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487217 | ||||||
| chr2:113487235
|
A | C | 1 | a0003c0003t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+5007A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487235 | ||||||
| chr2:113487238
|
A | T | 1 | a0003c0003t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+5010A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487238 | ||||||
| chr2:113487431
|
C | A | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+5203C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487431 | ||||||
| chr2:113487524
|
C | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.816+5296C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487524 | ||||||
| chr2:113487696
|
TATATGAC others(3): Show |
T | 9 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(6): Show | 11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+5471_816+5480d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113487696 | |||||
| chr2:113487716
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+5488A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487716 | ||||||
| chr2:113487776
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816+5548C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487776 | ||||||
| chr2:113487791
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.816+5563G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487791 | ||||||
| chr2:113487876
|
C | T | 1 | a0002c0002t0002g0190 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.816+5648C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487876 | ||||||
| chr2:113487922
|
T | C | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.816+5694T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487922 | ||||||
| chr2:113487932
|
G | A | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+5704G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487932 | ||||||
| chr2:113487968
|
G | A | 2 | a0002c0002t0002g0174a0002c0002t0002g0208 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.816+5740G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487968 | ||||||
| chr2:113487985
|
A | G | 84 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(81): Show | 94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.816+5757A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487985 | ||||||
| chr2:113488001
|
C | T | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.817-5756C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488001 | ||||||
| chr2:113488038
|
C | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-5719C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488038 | ||||||
| chr2:113488102
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5655A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488102 | ||||||
| chr2:113488183
|
T | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-5574T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488183 | ||||||
| chr2:113488208
|
C | A | 7 | a0002c0002t0002g0019a0002c0002t0002g0173a0002c0002t0002g0188others(4): Show | 7 | HG00423.hp1 HG01069.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-5549C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488208 | ||||||
| chr2:113488241
|
G | A | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-5516G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488241 | ||||||
| chr2:113488303
|
C | T | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5454C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488303 | ||||||
| chr2:113488384
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0098 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.817-5373C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488384 | ||||||
| chr2:113488603
|
TA | T | 94 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(91): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.817-5141delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113488603 | |||||
| chr2:113488605
|
A | T | 11 | a0001c0001t0001g0113a0002c0002t0002g0195a0002c0002t0002g0196others(8): Show | 13 | HG00140.hp2 HG01071.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-5152A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488605 | ||||||
| chr2:113488714
|
T | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5043T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488714 | ||||||
| chr2:113488870
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0113 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.817-4887G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488870 | ||||||
| chr2:113488897
|
G | A | 9 | a0002c0002t0002g0002a0002c0002t0002g0177a0002c0002t0002g0194others(6): Show | 10 | HG00438.hp2 HG00673.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-4860G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488897 | ||||||
| chr2:113488928
|
G | A | 1 | a0002c0002t0006g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-4829G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488928 | ||||||
| chr2:113488933
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-4824T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488933 | ||||||
| chr2:113488993
|
G | C | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-4764G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488993 | ||||||
| chr2:113489139
|
C | G | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.817-4618C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489139 | ||||||
| chr2:113489232
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-4525C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489232 | ||||||
| chr2:113489369
|
C | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-4388C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489369 | ||||||
| chr2:113489494
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.817-4263G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489494 | ||||||
| chr2:113489647
|
C | T | 1 | a0002c0002t0002g0190 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.817-4110C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489647 | ||||||
| chr2:113489746
|
C | A | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-4011C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489746 | ||||||
| chr2:113489851
|
C | T | 1 | a0002c0002t0006g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.817-3906C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489851 | ||||||
| chr2:113490082
|
A | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-3675A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490082 | ||||||
| chr2:113490412
|
C | CACAG | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-3342_817-3341i others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113490412 | |||||
| chr2:113490477
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-3280C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490477 | ||||||
| chr2:113490484
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-3273G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490484 | ||||||
| chr2:113490549
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.817-3208G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490549 | ||||||
| chr2:113490935
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-2822C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490935 | ||||||
| chr2:113491003
|
A | C | 1 | a0002c0002t0002g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.817-2754A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491003 | ||||||
| chr2:113491183
|
G | T | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-2574G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491183 | ||||||
| chr2:113491384
|
C | T | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.817-2373C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491384 | ||||||
| chr2:113491708
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-2049T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491708 | ||||||
| chr2:113491845
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1912T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491845 | ||||||
| chr2:113491866
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.817-1891G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491866 | ||||||
| chr2:113492017
|
G | A | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-1740G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492017 | ||||||
| chr2:113492052
|
A | G | 1 | a0002c0002t0002g0160 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-1705A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492052 | ||||||
| chr2:113492072
|
CAG | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1684_817-1683d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492072 | ||||||
| chr2:113492110
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1647T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492110 | ||||||
| chr2:113492188
|
C | T | 1 | a0002c0002t0006g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-1569C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492188 | ||||||
| chr2:113492211
|
C | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1546C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492211 | ||||||
| chr2:113492232
|
G | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1525G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492232 | ||||||
| chr2:113492242
|
T | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1515T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492242 | ||||||
| chr2:113492276
|
GAT | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1471_817-1470d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113492276 | |||||
| chr2:113492287
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1470A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492287 | ||||||
| chr2:113492301
|
A | G | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-1456A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492301 | ||||||
| chr2:113492305
|
C | T | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1452C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492305 | ||||||
| chr2:113492331
|
T | C | 1 | a0002c0002t0002g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.817-1426T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492331 | ||||||
| chr2:113492338
|
C | T | 1 | a0002c0002t0009g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.817-1419C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492338 | ||||||
| chr2:113492541
|
G | A | 18 | a0002c0002t0002g0007a0002c0002t0002g0018a0002c0002t0002g0153others(15): Show | 21 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.817-1216G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492541 | ||||||
| chr2:113492604
|
A | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1153A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492604 | ||||||
| chr2:113492629
|
A | G | 3 | a0001c0004t0003g0225a0001c0004t0003g0226a0001c0004t0003g0227 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.817-1128A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492629 | ||||||
| chr2:113492707
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1050A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492707 | ||||||
| chr2:113492708
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1049T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492708 | ||||||
| chr2:113492879
|
G | A | 166 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(163): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.817-878G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492879 | ||||||
| chr2:113493083
|
G | A | 87 | a0001c0001t0001g0050a0002c0002t0002g0001a0002c0002t0002g0002others(84): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.817-674G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493083 | ||||||
| chr2:113493111
|
A | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-646A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493111 | ||||||
| chr2:113493154
|
C | T | 1 | a0002c0002t0002g0218 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.817-603C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493154 | ||||||
| chr2:113493155
|
G | A | 18 | a0001c0004t0001g0232a0001c0004t0001g0233a0003c0003t0001g0008others(15): Show | 22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-602G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493155 | ||||||
| chr2:113493221
|
AT | A | 86 | a0001c0001t0001g0125a0002c0002t0002g0001a0002c0002t0002g0002others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-526delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113493221 | |||||
| chr2:113493241
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-516A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493241 | ||||||
| chr2:113493273
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-484C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493273 | ||||||
| chr2:113493388
|
A | G | 2 | a0001c0004t0001g0232a0001c0004t0001g0233 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.817-369A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493388 | ||||||
| chr2:113493461
|
G | A | 10 | a0001c0001t0001g0119a0003c0003t0001g0024a0003c0003t0001g0025others(7): Show | 12 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-296G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493461 | ||||||
| chr2:113493489
|
T | C | 84 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(81): Show | 94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.817-268T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493489 | ||||||
| chr2:113493523
|
AC | A | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-233delC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493523 | ||||||
| chr2:113493835
|
A | T | 1 | a0002c0002t0002g0201 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.885+10A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 12/14 | chr2 | 113493835 | ||||||
| chr2:113493848
|
A | T | 107 | a0001c0004t0001g0232a0001c0004t0001g0233a0001c0004t0003g0225others(104): Show | 121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.885+23A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 12/14 | chr2 | 113493848 | ||||||
| chr2:113494130
|
A | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.951+136A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494130 | ||||||
| chr2:113494302
|
T | G | 1 | a0002c0002t0006g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.951+308T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494302 | ||||||
| chr2:113494469
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.951+475A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494469 | ||||||
| chr2:113494599
|
A | G | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.952-521A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494599 | ||||||
| chr2:113494603
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-517T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494603 | ||||||
| chr2:113494619
|
A | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-501A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494619 | ||||||
| chr2:113494721
|
T | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-399T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494721 | ||||||
| chr2:113494753
|
T | G | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-367T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494753 | ||||||
| chr2:113494793
|
A | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0229a0003c0003t0001g0230others(4): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494793 | ||||||
| chr2:113494909
|
A | AT | 85 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(82): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.952-211_952-210ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494909 | ||||||
| chr2:113494991
|
T | G | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.952-129T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494991 | ||||||
| chr2:113495031
|
G | T | 2 | a0002c0002t0002g0186a0002c0002t0006g0206 | 2 | HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.952-89G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113495031 | ||||||
| chr2:113495258
|
G | C | 86 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0007others(83): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1081+9G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495258 | ||||||
| chr2:113495321
|
C | T | 104 | a0001c0004t0001g0232a0001c0004t0001g0233a0002c0002t0002g0001others(101): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1081+72C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495321 | ||||||
| chr2:113495613
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1082-24C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495613 | ||||||
| chr2:113495633
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.1082-4G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495633 |