| geneid | 80008 |
|---|---|
| ensemblid | ENSG00000121895.8 |
| hgncid | 26260 |
| symbol | TMEM156 |
| name | transmembrane protein 156 |
| refseq_nuc | NM_024943.3 |
| refseq_prot | NP_079219.1 |
| ensembl_nuc | ENST00000381938.4 |
| ensembl_prot | ENSP00000371364.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 38966744 |
| end | 39032409 |
| strand | - |
| ver | v1.2 |
| region | chr4:38966744-39032409 |
| region5000 | chr4:38961744-39037409 |
| regionname0 | TMEM156_chr4_38966744_39032409 |
| regionname5000 | TMEM156_chr4_38961744_39037409 |
| 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 | 296 | 253 | 68 | 55 | 98 | 5 | 25 | 68 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002 | 0/0 | 296 | 112 | 13 | 15 | 64 | 2 | 18 | 54 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0003 | 0/0 | 296 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004 | 0/0 | 296 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0005 | 0/0 | 296 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0006 | 0/0 | 296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 891 | 231 | 67 | 44 | 90 | 4 | 25 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0002 | 0/0 | 891 | 109 | 13 | 15 | 62 | 2 | 17 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0003 | 1/0 | 891 | 18 | 0 | 10 | 6 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0004 | 0/0 | 891 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0005 | 0/0 | 891 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0006 | 0/0 | 891 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0007 | 0/0 | 891 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0008 | 0/0 | 891 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0009 | 0/0 | 891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0010 | 0/0 | 891 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| c0011 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| 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 | 1/0 | 1033 | 163 | 29 | 35 | 66 | 7 | 25 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0002 | 0/0 | 1033 | 88 | 22 | 18 | 42 | 0 | 6 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0003 | 0/0 | 1034 | 54 | 7 | 14 | 27 | 0 | 6 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0004 | 0/0 | 1032 | 42 | 5 | 2 | 27 | 1 | 7 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0005 | 0/0 | 1036 | 20 | 18 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0006 | 0/0 | 1034 | 6 | 1 | 1 | 4 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0007 | 0/0 | 1033 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0008 | 0/0 | 1034 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0009 | 0/0 | 1033 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0010 | 0/0 | 1034 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0011 | 0/0 | 1033 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0012 | 0/0 | 1033 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0013 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0014 | 0/0 | 1033 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0015 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| t0016 | 0/1 | 1033 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0330 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 891 | 231 | 67 | 44 | 90 | 4 | 25 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003 | 1/0 | 891 | 18 | 0 | 10 | 6 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0009 | 0/0 | 891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0010 | 0/0 | 891 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0011 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002 | 0/0 | 891 | 109 | 13 | 15 | 62 | 2 | 17 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0007 | 0/0 | 891 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0003c0004 | 0/0 | 891 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004c0005 | 0/0 | 891 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0005c0006 | 0/0 | 891 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0006c0008 | 0/0 | 891 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1923 | 98 | 21 | 24 | 38 | 3 | 12 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0002 | 0/0 | 1923 | 46 | 16 | 8 | 17 | 0 | 5 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0003 | 0/0 | 1924 | 27 | 4 | 8 | 11 | 0 | 4 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0004 | 0/0 | 1922 | 28 | 3 | 2 | 18 | 1 | 4 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0005 | 0/0 | 1926 | 17 | 15 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0006 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0007 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0008 | 0/0 | 1924 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0009 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0010 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0012 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0013 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0014 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0015 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0001t0016 | 0/1 | 1923 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003t0001 | 1/0 | 1923 | 5 | 0 | 2 | 1 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003t0002 | 0/0 | 1923 | 7 | 0 | 5 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003t0003 | 0/0 | 1924 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003t0004 | 0/0 | 1922 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0003t0006 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0009t0001 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0009t0003 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0010t0003 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0001c0011t0001 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0001 | 0/0 | 1923 | 47 | 4 | 7 | 22 | 2 | 12 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0002 | 0/0 | 1923 | 30 | 4 | 5 | 20 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0003 | 0/0 | 1924 | 16 | 1 | 3 | 11 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0004 | 0/0 | 1922 | 12 | 2 | 0 | 7 | 0 | 3 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0005 | 0/0 | 1926 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0002t0006 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0007t0001 | 0/0 | 1923 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0002c0007t0003 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0003c0004t0001 | 0/0 | 1923 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0003c0004t0002 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0003c0004t0003 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004c0005t0001 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004c0005t0002 | 0/0 | 1923 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004c0005t0003 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0004c0005t0005 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0005c0006t0001 | 0/0 | 1923 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0005c0006t0003 | 0/0 | 1924 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0006c0008t0001 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0006c0008t0003 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| a0006c0008t0006 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | copy fasta | chr4 | 38961744 | 39037409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0005g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0008g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0012g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0015g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0001t0016g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0330 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0003t0006g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0009t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0009t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0010t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0001c0011t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0003g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0005g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0002t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0007t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0002c0007t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0003c0004t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0004c0005t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0005c0006t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0008t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0008t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| a0006c0008t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0068 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0079 | EUR | GBR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00280 | hp1 | a0005 | c0006 | t0001 | g0050 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0205 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0383 | EAS | CHS | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0284 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0203 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0360 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0332 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0242 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0331 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0361 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01074 | hp2 | a0005 | c0006 | t0001 | g0032 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0380 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0206 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0209 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01255 | hp2 | a0001 | c0010 | t0003 | g0004 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0261 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0365 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0342 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0121 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0366 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01981 | hp1 | a0001 | c0003 | t0006 | g0321 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02015 | hp2 | a0001 | c0001 | t0010 | g0092 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0151 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0226 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0245 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02071 | hp2 | a0003 | c0004 | t0002 | g0155 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0337 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02080 | hp1 | a0001 | c0009 | t0003 | g0071 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0128 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0367 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | CDX | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0215 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02300 | hp2 | a0002 | c0002 | t0003 | g0043 | AMR | PEL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02451 | hp1 | a0002 | c0002 | t0005 | g0166 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | KHV | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02622 | hp1 | a0004 | c0005 | t0005 | g0165 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02647 | hp2 | a0006 | c0008 | t0003 | g0338 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02738 | hp1 | a0005 | c0006 | t0003 | g0119 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02818 | hp1 | a0002 | c0002 | t0004 | g0010 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02818 | hp2 | a0006 | c0008 | t0001 | g0370 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0379 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0375 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0182 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0293 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0080 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02976 | hp1 | a0004 | c0005 | t0003 | g0212 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0373 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0189 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03139 | hp2 | a0004 | c0005 | t0002 | g0170 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03195 | hp1 | a0002 | c0002 | t0005 | g0381 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03225 | hp2 | a0006 | c0008 | t0006 | g0285 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0377 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0280 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03516 | hp1 | a0001 | c0011 | t0001 | g0198 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | ESN | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0371 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | GWD | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0251 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0250 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0336 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0328 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0042 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04184 | hp2 | a0002 | c0007 | t0001 | g0253 | SAS | BEB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0268 | SAS | STU | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18612 | hp1 | a0001 | c0001 | t0015 | g0093 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18747 | hp1 | a0001 | c0001 | t0012 | g0296 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18747 | hp2 | a0003 | c0004 | t0002 | g0113 | EAS | CHB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18940 | hp1 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18940 | hp2 | a0002 | c0002 | t0004 | g0149 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0356 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0257 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0230 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0091 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18948 | hp2 | a0001 | c0001 | t0014 | g0107 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0363 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0378 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18974 | hp1 | a0002 | c0002 | t0006 | g0018 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0325 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18986 | hp2 | a0001 | c0003 | t0004 | g0310 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0097 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18997 | hp2 | a0002 | c0002 | t0003 | g0382 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0341 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19009 | hp2 | a0002 | c0007 | t0003 | g0344 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19030 | hp2 | a0004 | c0005 | t0001 | g0118 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19058 | hp2 | a0002 | c0002 | t0004 | g0258 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19063 | hp1 | a0003 | c0004 | t0003 | g0016 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19063 | hp2 | a0002 | c0007 | t0003 | g0298 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19072 | hp1 | a0002 | c0002 | t0004 | g0103 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19082 | hp1 | a0003 | c0004 | t0002 | g0111 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19083 | hp2 | a0002 | c0002 | t0006 | g0064 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19087 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0239 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19091 | hp2 | a0001 | c0009 | t0001 | g0066 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0174 | AFR | YRI | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0279 | SAS | GIH | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG01123 | hp2 | a0005 | c0006 | t0001 | g0244 | AMR | CLM | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0005 | AFR | ACB | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | USA | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | USA | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0374 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | LWK | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0016 | g0106 | REF | REF | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0330 | REF | REF | TMEM156_chr4_38961744_39037409 | TMEM156 | chr4 | 38961744 | 39037409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38971071
|
T | C | 2 | a0001a0002 | 5 | HG02080.hp1 HG04184.hp2 NA19009.hp2 others(2): Show |
stop_retained_variant | LOW | c.890A>G | p.Ter297Ter | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/7 | 986/1923 | 890/891 | 297/296 | chr4 | 38971071 | ||
| chr4:38986345
|
C | T | 1 | a0005 | 4 | HG00280.hp1 HG01074.hp2 HG01123.hp2 others(1): Show |
missense_variant | MODERATE | c.814G>A | p.Val272Ile | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/7 | 910/1923 | 814/891 | 272/296 | chr4 | 38986345 | ||
| chr4:38988955
|
A | G | 1 | a0003 | 8 | HG02071.hp2 NA18747.hp2 NA18944.hp1 others(5): Show |
missense_variant | MODERATE | c.635T>C | p.Met212Thr | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/7 | 731/1923 | 635/891 | 212/296 | chr4 | 38988955 | ||
| chr4:38993781
|
A | T | 1 | a0006 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.576T>A | p.Asn192Lys | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/7 | 672/1923 | 576/891 | 192/296 | chr4 | 38993781 | ||
| chr4:38998685
|
A | G | 2 | a0002a0003 | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
missense_variant | MODERATE | c.313T>C | p.Ser105Pro | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/7 | 409/1923 | 313/891 | 105/296 | chr4 | 38998685 | ||
| chr4:38998855
|
T | C | 1 | a0004 | 6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.143A>G | p.Tyr48Cys | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/7 | 239/1923 | 143/891 | 48/296 | chr4 | 38998855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38971127
|
C | T | 1 | a0001c0011 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.834G>A | p.Thr278Thr | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/7 | 930/1923 | 834/891 | 278/296 | chr4 | 38971127 | ||
| chr4:38993754
|
T | C | 10 | a0001c0001a0001c0009a0001c0010others(7): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.603A>G | p.Leu201Leu | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/7 | 699/1923 | 603/891 | 201/296 | chr4 | 38993754 | ||
| chr4:39032272
|
C | T | 1 | a0001c0010 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.42G>A | p.Val14Val | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/7 | 138/1923 | 42/891 | 14/296 | chr4 | 39032272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38966782
|
G | A | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4288 | chr4 | 38966782 | |||||
| chr4:38966800
|
A | AT | 17 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(14): Show | 64 | HG00438.hp1 HG00673.hp1 HG00733.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*879dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4269 | chr4 | 38966800 | |||||
| chr4:38966800
|
AT | A | 4 | a0001c0001t0004a0001c0001t0015a0001c0003t0004others(1): Show | 43 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*879delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4269 | chr4 | 38966800 | |||||
| chr4:38966821
|
T | TTTG | 3 | a0001c0001t0005a0002c0002t0005a0004c0005t0005 | 20 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*858_*859insCAA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4248 | chr4 | 38966821 | |||||
| chr4:38966823
|
A | T | 11 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(8): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*857T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4247 | chr4 | 38966823 | |||||
| chr4:38966829
|
A | T | 1 | a0001c0001t0007 | 2 | HG02886.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*851T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4241 | chr4 | 38966829 | |||||
| chr4:38966907
|
T | G | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*773A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4163 | chr4 | 38966907 | |||||
| chr4:38966965
|
C | T | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4105 | chr4 | 38966965 | |||||
| chr4:38967026
|
C | T | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4044 | chr4 | 38967026 | |||||
| chr4:38967045
|
C | T | 1 | a0001c0001t0014 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 4025 | chr4 | 38967045 | |||||
| chr4:38967186
|
C | T | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3884 | chr4 | 38967186 | |||||
| chr4:38967280
|
A | C | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3790 | chr4 | 38967280 | |||||
| chr4:38967317
|
A | G | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3753 | chr4 | 38967317 | |||||
| chr4:38967355
|
T | C | 1 | a0001c0001t0008 | 2 | HG01884.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*325A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3715 | chr4 | 38967355 | |||||
| chr4:38967409
|
T | G | 1 | a0001c0001t0013 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3661 | chr4 | 38967409 | |||||
| chr4:38967411
|
C | T | 1 | a0001c0001t0013 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3659 | chr4 | 38967411 | |||||
| chr4:38967414
|
C | A | 1 | a0001c0001t0016 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3656 | chr4 | 38967414 | |||||
| chr4:38967616
|
C | T | 1 | a0001c0001t0012 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3454 | chr4 | 38967616 | |||||
| chr4:38967618
|
C | T | 1 | a0001c0001t0011 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3452 | chr4 | 38967618 | |||||
| chr4:38967623
|
C | T | 1 | a0001c0001t0010 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3447 | chr4 | 38967623 | |||||
| chr4:38967633
|
G | A | 1 | a0001c0001t0009 | 2 | HG03130.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*47C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 7/7 | 3437 | chr4 | 38967633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38967753
|
G | C | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-112C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967753 | ||||||
| chr4:38967806
|
G | A | 82 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0037others(79): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.*39-165C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967806 | ||||||
| chr4:38967973
|
A | G | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-332T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38967973 | ||||||
| chr4:38968078
|
C | T | 2 | a0001c0001t0001g0163a0004c0005t0001g0118 | 2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*39-437G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968078 | ||||||
| chr4:38968242
|
C | T | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-601G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968242 | ||||||
| chr4:38968289
|
G | T | 1 | a0002c0007t0003g0344 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.*39-648C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968289 | ||||||
| chr4:38968340
|
G | A | 1 | a0002c0002t0001g0336 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*39-699C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968340 | ||||||
| chr4:38968350
|
A | G | 1 | a0002c0002t0001g0308 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*39-709T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968350 | ||||||
| chr4:38968359
|
G | A | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-718C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968359 | ||||||
| chr4:38968402
|
A | C | 2 | a0001c0001t0011g0182a0006c0008t0001g0370 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.*39-761T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968402 | ||||||
| chr4:38968488
|
T | A | 1 | a0001c0001t0013g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-847A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968488 | ||||||
| chr4:38968499
|
G | A | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-858C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968499 | ||||||
| chr4:38968535
|
T | C | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-894A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968535 | ||||||
| chr4:38968550
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*39-909T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968550 | ||||||
| chr4:38968699
|
A | G | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*39-1058T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968699 | ||||||
| chr4:38968813
|
G | A | 1 | a0001c0001t0004g0318 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.*39-1172C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968813 | ||||||
| chr4:38968968
|
G | A | 5 | a0001c0001t0004g0191a0001c0001t0004g0196a0001c0001t0004g0214others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39-1327C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38968968 | ||||||
| chr4:38969086
|
A | G | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*39-1445T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969086 | ||||||
| chr4:38969093
|
G | C | 1 | a0001c0001t0013g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-1452C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969093 | ||||||
| chr4:38969094
|
C | G | 1 | a0001c0001t0013g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*39-1453G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969094 | ||||||
| chr4:38969125
|
G | C | 9 | a0001c0001t0004g0014a0001c0001t0004g0095a0001c0001t0004g0247others(6): Show | 9 | HG00597.hp2 HG00621.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.*39-1484C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969125 | ||||||
| chr4:38969437
|
A | G | 367 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(364): Show | 370 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.*38+1595T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969437 | ||||||
| chr4:38969448
|
GCAC | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1581_*38+1583d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969448 | ||||||
| chr4:38969544
|
T | C | 2 | a0001c0001t0002g0175a0001c0001t0002g0225 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*38+1488A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969544 | ||||||
| chr4:38969545
|
A | G | 2 | a0001c0001t0003g0238a0002c0002t0001g0137 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.*38+1487T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969545 | ||||||
| chr4:38969558
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1474G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969558 | ||||||
| chr4:38969597
|
T | C | 1 | a0002c0002t0004g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*38+1435A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969597 | ||||||
| chr4:38969599
|
G | A | 1 | a0006c0008t0003g0338 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*38+1433C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969599 | ||||||
| chr4:38969670
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1362C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969670 | ||||||
| chr4:38969700
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02818.hp2 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.*38+1332A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969700 | ||||||
| chr4:38969711
|
G | A | 1 | a0001c0001t0005g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*38+1321C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969711 | ||||||
| chr4:38969762
|
T | C | 103 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0001g0202others(100): Show | 104 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.*38+1270A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969762 | ||||||
| chr4:38969888
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+1144G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969888 | ||||||
| chr4:38969908
|
T | C | 1 | a0001c0003t0004g0023 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.*38+1124A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969908 | ||||||
| chr4:38969988
|
T | C | 9 | a0001c0001t0003g0178a0001c0001t0003g0195a0001c0001t0003g0220others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*38+1044A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38969988 | ||||||
| chr4:38970146
|
T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+886A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | ||||||
| chr4:38970146
|
T | TTG | 110 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0001g0202others(107): Show | 111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.*38+884_*38+885dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | ||||||
| chr4:38970146
|
T | TTGTG | 5 | a0001c0001t0002g0052a0001c0001t0002g0225a0002c0002t0002g0249others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.*38+882_*38+885dup others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970146 | ||||||
| chr4:38970148
|
G | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+884C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970148 | ||||||
| chr4:38970179
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+853G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970179 | ||||||
| chr4:38970182
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*38+850C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970182 | ||||||
| chr4:38970221
|
T | C | 1 | a0001c0001t0005g0380 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.*38+811A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970221 | ||||||
| chr4:38970264
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+768T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970264 | ||||||
| chr4:38970285
|
T | TC | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+746_*38+747ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970285 | ||||||
| chr4:38970287
|
G | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.*38+745C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970287 | ||||||
| chr4:38970381
|
T | A | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*38+651A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970381 | ||||||
| chr4:38970652
|
C | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0171a0001c0001t0001g0176others(18): Show | 21 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.*38+380G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970652 | ||||||
| chr4:38970754
|
C | T | 11 | a0001c0001t0001g0222a0001c0001t0001g0288a0001c0001t0003g0178others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.*38+278G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970754 | ||||||
| chr4:38970781
|
A | G | 1 | a0001c0001t0004g0355 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*38+251T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970781 | ||||||
| chr4:38970872
|
G | A | 4 | a0001c0001t0002g0192a0001c0001t0002g0374a0004c0005t0002g0170others(1): Show | 4 | HG03098.hp2 HG03139.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.*38+160C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 6/6 | chr4 | 38970872 | ||||||
| chr4:38971173
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-36T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971173 | ||||||
| chr4:38971200
|
T | G | 1 | a0002c0002t0001g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.824-63A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971200 | ||||||
| chr4:38971360
|
G | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-223C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971360 | ||||||
| chr4:38971475
|
T | G | 1 | a0002c0002t0004g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824-338A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971475 | ||||||
| chr4:38971795
|
A | AT | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-659dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971795 | ||||||
| chr4:38971812
|
A | G | 285 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(282): Show | 288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.824-675T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971812 | ||||||
| chr4:38971820
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-683C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971820 | ||||||
| chr4:38971977
|
C | T | 2 | a0001c0001t0004g0014a0002c0002t0004g0258 | 2 | NA19057.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.824-840G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38971977 | ||||||
| chr4:38972145
|
C | T | 2 | a0002c0002t0001g0281a0002c0002t0001g0283 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.824-1008G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972145 | ||||||
| chr4:38972211
|
G | A | 2 | a0001c0001t0005g0286a0001c0001t0005g0371 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.824-1074C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972211 | ||||||
| chr4:38972242
|
A | AT | 12 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0001g0274others(9): Show | 12 | HG00423.hp1 HG01243.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1106dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.824-1116_824-1106d others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0349others(1): Show | 4 | HG03942.hp1 NA18962.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1117_824-1106d others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
AT | A | 30 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0188others(27): Show | 30 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.824-1106delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
ATT | A | 23 | a0001c0001t0001g0171a0001c0001t0001g0185a0001c0001t0001g0287others(20): Show | 23 | HG00438.hp1 HG00621.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-1107_824-1106d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
ATTT | A | 119 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0029others(116): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.824-1108_824-1106d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
ATTTT | A | 99 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0002g0011others(96): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.824-1109_824-1106d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972242
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0004g0191a0001c0001t0004g0196a0001c0001t0004g0214others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1115_824-1106d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972242 | ||||||
| chr4:38972316
|
C | T | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.824-1179G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972316 | ||||||
| chr4:38972348
|
G | A | 1 | a0001c0003t0002g0006 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.824-1211C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972348 | ||||||
| chr4:38972447
|
C | T | 1 | a0001c0001t0003g0311 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.824-1310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972447 | ||||||
| chr4:38972564
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.824-1427A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972564 | ||||||
| chr4:38972650
|
C | CA | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1514_824-1513i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972650 | ||||||
| chr4:38972658
|
C | G | 1 | a0001c0001t0003g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-1521G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972658 | ||||||
| chr4:38972838
|
A | C | 105 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0001g0202others(102): Show | 106 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.824-1701T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972838 | ||||||
| chr4:38972884
|
T | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1747A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38972884 | ||||||
| chr4:38973126
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-1989C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973126 | ||||||
| chr4:38973156
|
T | C | 2 | a0001c0001t0004g0247a0002c0002t0004g0123 | 2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.824-2019A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973156 | ||||||
| chr4:38973389
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2252A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973389 | ||||||
| chr4:38973433
|
T | C | 5 | a0001c0001t0004g0191a0001c0001t0004g0196a0001c0001t0004g0214others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2296A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973433 | ||||||
| chr4:38973476
|
A | G | 8 | a0001c0001t0002g0072a0001c0001t0002g0353a0001c0001t0006g0314others(5): Show | 8 | HG00609.hp2 HG02083.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-2339T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973476 | ||||||
| chr4:38973482
|
T | C | 1 | a0002c0002t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-2345A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973482 | ||||||
| chr4:38973526
|
A | C | 1 | a0001c0001t0004g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.824-2389T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973526 | ||||||
| chr4:38973639
|
C | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2502G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973639 | ||||||
| chr4:38973677
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2540G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973677 | ||||||
| chr4:38973922
|
A | G | 5 | a0001c0001t0004g0191a0001c0001t0004g0196a0001c0001t0004g0214others(2): Show | 5 | HG01109.hp2 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2785T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38973922 | ||||||
| chr4:38974058
|
C | T | 3 | a0002c0002t0001g0101a0002c0002t0001g0281a0002c0002t0001g0283 | 3 | HG02735.hp2 HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.824-2921G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | ||||||
| chr4:38974058
|
CGT | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0100others(51): Show | 54 | HG00099.hp1 HG01255.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.824-2923_824-2922d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | ||||||
| chr4:38974058
|
CGTGT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0085others(8): Show | 11 | HG02129.hp1 HG02895.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.824-2925_824-2922d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | ||||||
| chr4:38974058
|
CGTGTGT | C | 235 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0029others(232): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.824-2927_824-2922d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974058 | ||||||
| chr4:38974207
|
C | CT | 110 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0039others(107): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.824-3071dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974207 | ||||||
| chr4:38974207
|
CT | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0222others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.824-3071delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974207 | ||||||
| chr4:38974209
|
T | C | 9 | a0001c0001t0002g0031a0001c0001t0002g0180a0001c0001t0002g0343others(6): Show | 9 | HG00741.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-3072A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974209 | ||||||
| chr4:38974519
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3382C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974519 | ||||||
| chr4:38974674
|
A | AT | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0150others(39): Show | 42 | HG00099.hp1 HG01167.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.824-3538dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | ||||||
| chr4:38974674
|
A | ATT | 16 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-3539_824-3538d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | ||||||
| chr4:38974674
|
AT | A | 111 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0037others(108): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.824-3538delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974674 | ||||||
| chr4:38974710
|
C | T | 2 | a0001c0001t0001g0037a0006c0008t0003g0338 | 2 | HG02647.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.824-3573G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974710 | ||||||
| chr4:38974874
|
T | A | 1 | a0006c0008t0003g0338 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.824-3737A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974874 | ||||||
| chr4:38974898
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.824-3761G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974898 | ||||||
| chr4:38974913
|
A | T | 284 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(281): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.824-3776T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974913 | ||||||
| chr4:38974915
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3778G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974915 | ||||||
| chr4:38974950
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0339 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.824-3813C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974950 | ||||||
| chr4:38974963
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3826C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38974963 | ||||||
| chr4:38975005
|
G | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3868C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975005 | ||||||
| chr4:38975029
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0005g0164a0001c0001t0005g0177others(3): Show | 6 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-3892G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975029 | ||||||
| chr4:38975189
|
T | C | 2 | a0001c0001t0001g0368a0005c0006t0001g0244 | 2 | HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.824-4052A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975189 | ||||||
| chr4:38975223
|
T | C | 1 | a0001c0001t0009g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-4086A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975223 | ||||||
| chr4:38975372
|
CTTTTTTC others(6): Show |
C | 11 | a0001c0001t0001g0222a0001c0001t0001g0288a0001c0001t0003g0178others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.824-4248_824-4236d others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975372 | ||||||
| chr4:38975381
|
TTTC | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-4247_824-4245d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975381 | ||||||
| chr4:38975383
|
TC | T | 100 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0002g0011others(97): Show | 101 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.824-4247delG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975383 | ||||||
| chr4:38975384
|
C | T | 2 | a0002c0002t0002g0108a0003c0004t0002g0113 | 2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.824-4247G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975384 | ||||||
| chr4:38975384
|
CT | C | 118 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0029others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.824-4248delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975384 | ||||||
| chr4:38975416
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0306 | 2 | HG01256.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.824-4279A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975416 | ||||||
| chr4:38975508
|
G | A | 108 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0085others(105): Show | 109 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.824-4371C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975508 | ||||||
| chr4:38975555
|
A | G | 111 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0085others(108): Show | 112 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.824-4418T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975555 | ||||||
| chr4:38975617
|
G | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0085others(107): Show | 111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.824-4480C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975617 | ||||||
| chr4:38975722
|
A | C | 1 | a0001c0001t0001g0333 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.824-4585T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975722 | ||||||
| chr4:38975744
|
C | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0222others(24): Show | 27 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.824-4607G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975744 | ||||||
| chr4:38975746
|
C | A | 110 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0085others(107): Show | 111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.824-4609G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975746 | ||||||
| chr4:38975908
|
G | C | 4 | a0002c0002t0001g0012a0002c0002t0001g0236a0003c0004t0001g0115others(1): Show | 4 | NA18951.hp1 NA18955.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-4771C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975908 | ||||||
| chr4:38975912
|
G | A | 1 | a0002c0002t0002g0356 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.824-4775C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975912 | ||||||
| chr4:38975941
|
A | G | 1 | a0001c0001t0004g0354 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.824-4804T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38975941 | ||||||
| chr4:38976012
|
C | A | 7 | a0001c0001t0001g0171a0001c0001t0005g0164a0001c0001t0005g0177others(4): Show | 7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-4875G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976012 | ||||||
| chr4:38976013
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0163others(15): Show | 18 | HG00099.hp1 HG01255.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.824-4876C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976013 | ||||||
| chr4:38976084
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0188others(14): Show | 17 | HG01255.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.824-4947G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976084 | ||||||
| chr4:38976275
|
G | A | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.824-5138C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976275 | ||||||
| chr4:38976289
|
C | CA | 10 | a0001c0001t0001g0120a0001c0001t0001g0294a0001c0001t0002g0208others(7): Show | 10 | HG00597.hp1 HG01361.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-5153dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | ||||||
| chr4:38976289
|
CA | C | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0021others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.824-5153delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | ||||||
| chr4:38976289
|
CAA | C | 92 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0001g0349others(89): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.824-5154_824-5153d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | ||||||
| chr4:38976289
|
CAAA | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(17): Show | 21 | HG01109.hp2 HG02129.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.824-5155_824-5153d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976289 | ||||||
| chr4:38976354
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(10): Show | 13 | HG01109.hp2 HG02129.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-5217C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976354 | ||||||
| chr4:38976357
|
G | A | 103 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0002g0011others(100): Show | 104 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.824-5220C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976357 | ||||||
| chr4:38976381
|
A | T | 115 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0029others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.824-5244T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976381 | ||||||
| chr4:38976408
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0133others(7): Show | 10 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.824-5271G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976408 | ||||||
| chr4:38976551
|
C | T | 97 | a0001c0001t0001g0075a0001c0001t0001g0201a0001c0001t0002g0011others(94): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.824-5414G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976551 | ||||||
| chr4:38976563
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0201a0002c0002t0003g0239 | 3 | NA18941.hp1 NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.824-5426C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976563 | ||||||
| chr4:38976669
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0001g0232others(4): Show | 7 | HG02129.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-5532T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976669 | ||||||
| chr4:38976807
|
C | G | 148 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0060others(145): Show | 149 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.824-5670G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976807 | ||||||
| chr4:38976890
|
T | TTTG | 169 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0044others(166): Show | 170 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.824-5756_824-5754d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | ||||||
| chr4:38976890
|
T | TTTGTTGT others(2): Show |
30 | a0001c0001t0001g0202a0001c0001t0003g0265a0001c0001t0004g0014others(27): Show | 31 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-5762_824-5754d others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | ||||||
| chr4:38976890
|
T | TTTGTTGT others(8): Show |
1 | a0001c0001t0004g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.824-5768_824-5754d others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | ||||||
| chr4:38976890
|
TTTG | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0163others(16): Show | 19 | HG00099.hp1 HG01255.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.824-5756_824-5754d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | ||||||
| chr4:38976890
|
TTTGTTG | T | 68 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0037others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.824-5759_824-5754d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976890 | ||||||
| chr4:38976980
|
A | T | 2 | a0001c0001t0007g0062a0001c0001t0007g0161 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.824-5843T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38976980 | ||||||
| chr4:38977066
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-5929C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977066 | ||||||
| chr4:38977072
|
T | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(30): Show | 33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5935A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977072 | ||||||
| chr4:38977117
|
C | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(29): Show | 32 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-5980G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977117 | ||||||
| chr4:38977125
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(30): Show | 33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5988T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977125 | ||||||
| chr4:38977126
|
AACT | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(30): Show | 33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5992_824-5990d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977126 | ||||||
| chr4:38977130
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(30): Show | 33 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-5993G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977130 | ||||||
| chr4:38977148
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0005g0164a0001c0001t0005g0177others(3): Show | 6 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-6011C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977148 | ||||||
| chr4:38977208
|
A | C | 1 | a0002c0002t0001g0259 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.824-6071T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977208 | ||||||
| chr4:38977293
|
G | A | 1 | a0001c0001t0005g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.824-6156C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977293 | ||||||
| chr4:38977359
|
A | G | 1 | a0002c0002t0001g0240 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.824-6222T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977359 | ||||||
| chr4:38977433
|
A | T | 41 | a0001c0001t0001g0202a0001c0001t0003g0265a0001c0001t0004g0014others(38): Show | 42 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.824-6296T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977433 | ||||||
| chr4:38977492
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0188others(4): Show | 7 | HG00099.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-6355A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977492 | ||||||
| chr4:38977524
|
C | T | 3 | a0001c0001t0009g0189a0001c0001t0011g0182a0006c0008t0001g0370 | 3 | HG02818.hp2 HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.824-6387G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977524 | ||||||
| chr4:38977630
|
A | G | 1 | a0001c0001t0009g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-6493T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977630 | ||||||
| chr4:38977786
|
G | C | 1 | a0002c0002t0004g0149 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-6649C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977786 | ||||||
| chr4:38977841
|
A | G | 3 | a0001c0001t0005g0054a0001c0001t0005g0224a0004c0005t0005g0165 | 3 | HG01243.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.824-6704T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977841 | ||||||
| chr4:38977937
|
T | A | 348 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.824-6800A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977937 | ||||||
| chr4:38977946
|
C | T | 1 | a0002c0002t0001g0236 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.824-6809G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977946 | ||||||
| chr4:38977987
|
A | G | 139 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0026others(136): Show | 141 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(138): Show |
intron_variant | MODIFIER | c.824-6850T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38977987 | ||||||
| chr4:38978049
|
A | G | 2 | a0001c0001t0001g0021a0002c0002t0004g0251 | 2 | HG01361.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.824-6912T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978049 | ||||||
| chr4:38978062
|
T | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0160a0001c0001t0001g0162others(29): Show | 32 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.824-6925A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978062 | ||||||
| chr4:38978191
|
T | A | 42 | a0001c0001t0001g0081a0001c0001t0001g0140a0001c0001t0001g0143others(39): Show | 42 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.824-7054A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978191 | ||||||
| chr4:38978258
|
A | G | 127 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(124): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.824-7121T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978258 | ||||||
| chr4:38978267
|
T | A | 1 | a0001c0001t0004g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824-7130A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978267 | ||||||
| chr4:38978267
|
T | TA | 96 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0029others(93): Show | 96 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.824-7131dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978267 | ||||||
| chr4:38978305
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0160a0001c0001t0001g0162others(2): Show | 5 | HG02451.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-7168A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978305 | ||||||
| chr4:38978316
|
C | A | 368 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(365): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.824-7179G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978316 | ||||||
| chr4:38978376
|
T | C | 3 | a0001c0001t0001g0346a0001c0001t0004g0069a0001c0001t0004g0153 | 3 | HG03704.hp2 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.824-7239A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978376 | ||||||
| chr4:38978387
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-7250G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978387 | ||||||
| chr4:38978444
|
T | C | 251 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(248): Show | 254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.824-7307A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978444 | ||||||
| chr4:38978503
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.824-7366G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978503 | ||||||
| chr4:38978521
|
C | T | 152 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0040others(149): Show | 153 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.824-7384G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978521 | ||||||
| chr4:38978566
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0287a0001c0001t0004g0055others(2): Show | 5 | HG02027.hp2 NA18957.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-7429G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978566 | ||||||
| chr4:38978721
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0201 | 2 | NA18961.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.824-7584T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978721 | ||||||
| chr4:38978749
|
T | C | 2 | a0001c0001t0002g0136a0001c0001t0009g0189 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.823+7587A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978749 | ||||||
| chr4:38978908
|
G | A | 1 | a0001c0001t0004g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.823+7428C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38978908 | ||||||
| chr4:38979082
|
A | G | 2 | a0003c0004t0001g0229a0003c0004t0001g0230 | 2 | NA18944.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.823+7254T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979082 | ||||||
| chr4:38979307
|
A | C | 13 | a0001c0001t0001g0140a0001c0001t0001g0160a0001c0001t0001g0162others(10): Show | 13 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+7029T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979307 | ||||||
| chr4:38979379
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0004g0217 | 2 | NA18961.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.823+6957C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979379 | ||||||
| chr4:38979451
|
T | C | 1 | a0001c0001t0008g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.823+6885A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979451 | ||||||
| chr4:38979471
|
T | C | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+6865A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979471 | ||||||
| chr4:38979646
|
T | G | 1 | a0001c0001t0005g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823+6690A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979646 | ||||||
| chr4:38979683
|
T | G | 1 | a0001c0001t0004g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.823+6653A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979683 | ||||||
| chr4:38979775
|
A | G | 1 | a0002c0002t0001g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.823+6561T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979775 | ||||||
| chr4:38979806
|
A | C | 1 | a0001c0001t0004g0303 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.823+6530T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979806 | ||||||
| chr4:38979821
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0013g0293 | 2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.823+6515T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979821 | ||||||
| chr4:38979822
|
G | C | 58 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(55): Show | 58 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.823+6514C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979822 | ||||||
| chr4:38979865
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0002g0011a0001c0001t0003g0220others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+6471G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979865 | ||||||
| chr4:38979990
|
C | A | 1 | a0001c0001t0005g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+6346G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38979990 | ||||||
| chr4:38980040
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.823+6296T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980040 | ||||||
| chr4:38980120
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+6216T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980120 | ||||||
| chr4:38980185
|
T | TA | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0094others(22): Show | 25 | HG00423.hp1 HG01081.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.823+6150dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | ||||||
| chr4:38980185
|
T | TAA | 52 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.823+6149_823+6150d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | ||||||
| chr4:38980185
|
TA | T | 30 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(27): Show | 31 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.823+6150delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980185 | ||||||
| chr4:38980205
|
A | G | 1 | a0001c0001t0007g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.823+6131T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980205 | ||||||
| chr4:38980272
|
T | C | 1 | a0001c0001t0008g0377 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+6064A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38980272 | ||||||
| chr4:38981033
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.823+5303C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981033 | ||||||
| chr4:38981131
|
T | C | 46 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+5205A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981131 | ||||||
| chr4:38981135
|
C | T | 194 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.823+5201G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981135 | ||||||
| chr4:38981174
|
T | C | 3 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0013g0293 | 3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.823+5162A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981174 | ||||||
| chr4:38981223
|
G | C | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+5113C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981223 | ||||||
| chr4:38981225
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823+5111C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981225 | ||||||
| chr4:38981240
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+5096G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981240 | ||||||
| chr4:38981348
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+4988T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981348 | ||||||
| chr4:38981363
|
G | A | 195 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.823+4973C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981363 | ||||||
| chr4:38981410
|
A | G | 1 | a0002c0002t0002g0363 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.823+4926T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981410 | ||||||
| chr4:38981436
|
T | G | 1 | a0002c0002t0003g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.823+4900A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981436 | ||||||
| chr4:38981470
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.823+4866T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981470 | ||||||
| chr4:38981493
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+4843T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981493 | ||||||
| chr4:38981524
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0140others(30): Show | 33 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+4812C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981524 | ||||||
| chr4:38981672
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+4664T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981672 | ||||||
| chr4:38981943
|
G | A | 10 | a0001c0001t0001g0140a0001c0001t0001g0160a0001c0001t0001g0162others(7): Show | 10 | HG01255.hp2 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+4393C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981943 | ||||||
| chr4:38981993
|
A | G | 5 | a0002c0002t0001g0236a0002c0002t0001g0283a0002c0002t0002g0237others(2): Show | 5 | HG00733.hp2 HG02083.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+4343T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38981993 | ||||||
| chr4:38982016
|
G | A | 7 | a0002c0002t0001g0169a0004c0005t0001g0118a0004c0005t0001g0226others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+4320C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982016 | ||||||
| chr4:38982092
|
C | T | 56 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0140others(53): Show | 56 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.823+4244G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982092 | ||||||
| chr4:38982140
|
C | A | 3 | a0001c0001t0001g0138a0001c0001t0002g0070a0001c0001t0002g0076 | 3 | NA18969.hp2 NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.823+4196G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982140 | ||||||
| chr4:38982140
|
C | G | 154 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.823+4196G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982140 | ||||||
| chr4:38982189
|
C | T | 43 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.823+4147G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982189 | ||||||
| chr4:38982223
|
G | A | 156 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.823+4113C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982223 | ||||||
| chr4:38982305
|
T | C | 161 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.823+4031A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982305 | ||||||
| chr4:38982385
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+3951G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982385 | ||||||
| chr4:38982899
|
A | G | 1 | a0004c0005t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823+3437T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38982899 | ||||||
| chr4:38983077
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+3259G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983077 | ||||||
| chr4:38983094
|
G | C | 1 | a0002c0002t0001g0266 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823+3242C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983094 | ||||||
| chr4:38983126
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.823+3210G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983126 | ||||||
| chr4:38983170
|
C | G | 1 | a0001c0001t0002g0147 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.823+3166G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983170 | ||||||
| chr4:38983205
|
T | C | 160 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+3131A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983205 | ||||||
| chr4:38983232
|
G | A | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.823+3104C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983232 | ||||||
| chr4:38983451
|
T | C | 5 | a0001c0001t0001g0139a0005c0006t0001g0032a0005c0006t0001g0050others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2885A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983451 | ||||||
| chr4:38983514
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+2822A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983514 | ||||||
| chr4:38983748
|
A | T | 3 | a0001c0001t0001g0171a0001c0001t0005g0187a0001c0001t0008g0377 | 3 | HG03453.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823+2588T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983748 | ||||||
| chr4:38983855
|
C | T | 47 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(44): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.823+2481G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38983855 | ||||||
| chr4:38984082
|
G | C | 135 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.823+2254C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984082 | ||||||
| chr4:38984185
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.823+2151G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984185 | ||||||
| chr4:38984199
|
G | A | 2 | a0002c0002t0003g0245a0002c0002t0003g0367 | 2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.823+2137C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984199 | ||||||
| chr4:38984325
|
T | TTC | 6 | a0002c0002t0001g0169a0004c0005t0001g0226a0004c0005t0002g0170others(3): Show | 6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2009_823+2010d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984325 | ||||||
| chr4:38984331
|
CTG | C | 20 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(17): Show | 20 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+2003_823+2004d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984331 | ||||||
| chr4:38984333
|
G | C | 62 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0085others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.823+2003C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984333 | ||||||
| chr4:38984333
|
G | GTC | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0002c0002t0001g0291 | 3 | HG02451.hp2 HG03471.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.823+2001_823+2002d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984333 | ||||||
| chr4:38984335
|
C | G | 61 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0085others(58): Show | 61 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.823+2001G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984335 | ||||||
| chr4:38984337
|
C | G | 20 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(17): Show | 20 | HG01167.hp1 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+1999G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984337 | ||||||
| chr4:38984345
|
C | CTGTGTGT others(1): Show |
12 | a0001c0001t0001g0127a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+1990_823+1991i others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | ||||||
| chr4:38984345
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.823+1990_823+1991i others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | ||||||
| chr4:38984345
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+1990_823+1991i others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | ||||||
| chr4:38984345
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0005g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1990_823+1991i others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984345 | ||||||
| chr4:38984347
|
C | G | 18 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.823+1989G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | ||||||
| chr4:38984347
|
CTCTGTG | C | 40 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.823+1983_823+1988d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | ||||||
| chr4:38984347
|
CTCTGTGT others(3): Show |
C | 2 | a0001c0001t0016g0106a0004c0005t0001g0118 | 2 | NA19030.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.823+1979_823+1988d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984347 | ||||||
| chr4:38984349
|
C | CTG | 22 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0003t0001g0337others(19): Show | 23 | HG00621.hp2 HG01934.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+1985_823+1986d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
C | CTGTG | 3 | a0002c0002t0002g0255a0003c0004t0001g0229a0003c0004t0001g0230 | 3 | HG02523.hp2 NA18944.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.823+1983_823+1986d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
C | G | 23 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(20): Show | 24 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.823+1987G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
CTG | C | 9 | a0001c0001t0002g0025a0001c0001t0004g0263a0001c0001t0005g0270others(6): Show | 9 | HG00609.hp2 HG01175.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1985_823+1986d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
CTGTG | C | 89 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(86): Show | 89 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.823+1983_823+1986d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
CTGTGTG | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+1981_823+1986d others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0171others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+1979_823+1986d others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984349
|
CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0004g0191a0001c0001t0004g0214a0001c0001t0004g0221others(1): Show | 4 | HG01109.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1977_823+1986d others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984349 | ||||||
| chr4:38984351
|
G | C | 54 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(51): Show | 54 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.823+1985C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984351 | ||||||
| chr4:38984353
|
G | C | 48 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(45): Show | 48 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.823+1983C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984353 | ||||||
| chr4:38984355
|
G | C | 42 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(39): Show | 42 | HG00423.hp1 HG01167.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.823+1981C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984355 | ||||||
| chr4:38984357
|
G | C | 3 | a0001c0001t0001g0254a0001c0001t0003g0088a0001c0001t0003g0378 | 3 | HG02293.hp1 HG03942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.823+1979C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984357 | ||||||
| chr4:38984359
|
G | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0171others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1977C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984359 | ||||||
| chr4:38984361
|
G | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(7): Show | 10 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+1975C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984361 | ||||||
| chr4:38984377
|
GTGTGTGT | G | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+1952_823+1958d others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984377 | ||||||
| chr4:38984477
|
G | GAC | 72 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(69): Show | 72 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.823+1857_823+1858d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984477 | ||||||
| chr4:38984563
|
C | T | 5 | a0002c0002t0001g0137a0002c0002t0001g0268a0002c0002t0004g0042others(2): Show | 5 | HG03669.hp2 HG03688.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1773G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984563 | ||||||
| chr4:38984614
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0136others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1722T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984614 | ||||||
| chr4:38984618
|
T | G | 256 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.823+1718A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984618 | ||||||
| chr4:38984685
|
A | G | 6 | a0002c0002t0001g0169a0004c0005t0001g0226a0004c0005t0002g0170others(3): Show | 6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+1651T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984685 | ||||||
| chr4:38984811
|
C | T | 2 | a0002c0002t0001g0046a0002c0002t0002g0326 | 2 | NA19000.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.823+1525G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984811 | ||||||
| chr4:38984997
|
C | CA | 159 | a0001c0001t0001g0026a0001c0001t0001g0060a0001c0001t0001g0061others(156): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+1338_823+1339i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38984997 | ||||||
| chr4:38985152
|
G | T | 115 | a0001c0001t0001g0026a0001c0001t0001g0109a0001c0001t0001g0124others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.823+1184C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985152 | ||||||
| chr4:38985159
|
G | C | 6 | a0001c0001t0001g0013a0001c0001t0004g0014a0001c0001t0004g0295others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+1177C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985159 | ||||||
| chr4:38985211
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823+1125G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985211 | ||||||
| chr4:38985443
|
C | T | 32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0140others(29): Show | 32 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.823+893G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985443 | ||||||
| chr4:38985475
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.823+861C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985475 | ||||||
| chr4:38985554
|
C | T | 4 | a0002c0002t0001g0137a0002c0002t0001g0268a0002c0002t0004g0042others(1): Show | 4 | HG03688.hp1 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+782G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985554 | ||||||
| chr4:38985616
|
A | G | 15 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(12): Show | 16 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+720T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985616 | ||||||
| chr4:38985647
|
C | T | 1 | a0002c0002t0002g0249 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.823+689G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985647 | ||||||
| chr4:38985702
|
T | C | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.823+634A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985702 | ||||||
| chr4:38985795
|
G | C | 1 | a0001c0001t0005g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.823+541C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985795 | ||||||
| chr4:38985812
|
A | C | 3 | a0001c0001t0001g0173a0001c0001t0002g0011a0001c0001t0005g0007 | 3 | HG02717.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.823+524T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985812 | ||||||
| chr4:38985863
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0002g0289 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.823+473A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985863 | ||||||
| chr4:38985927
|
T | C | 1 | a0001c0001t0005g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+409A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38985927 | ||||||
| chr4:38986083
|
C | G | 1 | a0001c0001t0005g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+253G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986083 | ||||||
| chr4:38986089
|
A | G | 11 | a0001c0001t0001g0176a0001c0001t0002g0031a0001c0001t0002g0269others(8): Show | 11 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+247T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986089 | ||||||
| chr4:38986090
|
C | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0053others(45): Show | 49 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.823+246G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986090 | ||||||
| chr4:38986205
|
A | G | 3 | a0002c0002t0001g0079a0002c0002t0001g0101a0002c0002t0001g0145 | 3 | HG00140.hp2 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.823+131T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 5/6 | chr4 | 38986205 | ||||||
| chr4:38986462
|
C | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(26): Show | 29 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.740-43G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986462 | ||||||
| chr4:38986512
|
A | G | 9 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(6): Show | 9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-93T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986512 | ||||||
| chr4:38986604
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0005g0187 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-185G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986604 | ||||||
| chr4:38986618
|
C | T | 1 | a0001c0001t0004g0354 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.740-199G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986618 | ||||||
| chr4:38986679
|
A | G | 3 | a0001c0001t0002g0184a0001c0001t0008g0342a0001c0001t0008g0377 | 3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-260T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986679 | ||||||
| chr4:38986729
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0013g0293 | 3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.740-310T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986729 | ||||||
| chr4:38986780
|
C | A | 9 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(6): Show | 9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-361G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986780 | ||||||
| chr4:38986786
|
C | T | 41 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.740-367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986786 | ||||||
| chr4:38986787
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.740-368C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986787 | ||||||
| chr4:38986807
|
CAA | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0150others(11): Show | 14 | HG01952.hp2 HG01981.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-390_740-389del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAA | C | 43 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.740-391_740-389del others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAA | C | 65 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0073others(62): Show | 65 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.740-392_740-389del others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAA | C | 47 | a0001c0001t0001g0024a0001c0001t0001g0158a0001c0001t0001g0176others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.740-393_740-389del others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAA | C | 25 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0173others(22): Show | 25 | HG01070.hp1 HG01256.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.740-394_740-389del others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0100others(20): Show | 24 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.740-395_740-389del others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0005g0177a0001c0001t0005g0187a0001c0001t0005g0270others(12): Show | 15 | HG00741.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-396_740-389del others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(2): Show |
C | 37 | a0001c0001t0001g0026a0002c0002t0001g0030a0002c0002t0001g0034others(34): Show | 38 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.740-397_740-389del others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(3): Show |
C | 50 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0002g0353others(47): Show | 51 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.740-398_740-389del others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(4): Show |
C | 8 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0181others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.740-399_740-389del others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(5): Show |
C | 2 | a0006c0008t0003g0338a0006c0008t0006g0285 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.740-400_740-389del others(12): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0184a0001c0001t0008g0342a0001c0001t0008g0377 | 3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-401_740-389del others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0136others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-403_740-389del others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0292a0001c0001t0002g0228a0001c0001t0013g0293 | 3 | HG02922.hp2 HG02965.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.740-404_740-389del others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.740-405_740-389del others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(12): Show |
C | 9 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0120others(6): Show | 9 | HG00099.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-407_740-389del others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(13): Show |
C | 4 | a0001c0001t0001g0157a0001c0001t0002g0147a0001c0001t0010g0092others(1): Show | 4 | HG02015.hp2 NA18612.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-408_740-389del others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(14): Show |
C | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG01993.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-409_740-389del others(21): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(15): Show |
C | 3 | a0001c0001t0002g0020a0001c0001t0002g0112a0001c0001t0004g0095 | 3 | HG00609.hp1 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.740-410_740-389del others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.740-411_740-389del others(23): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(18): Show |
C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.740-413_740-389del others(25): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(19): Show |
C | 1 | a0002c0002t0002g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.740-414_740-389del others(26): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.740-415_740-389del others(27): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(22): Show |
C | 2 | a0002c0002t0001g0236a0002c0002t0004g0123 | 2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.740-417_740-389del others(29): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986807
|
CAAAAAAA others(25): Show |
C | 1 | a0001c0001t0001g0316 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740-420_740-389del others(32): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986807 | ||||||
| chr4:38986829
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0136others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-410T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986829 | ||||||
| chr4:38986882
|
T | C | 2 | a0001c0003t0002g0206a0001c0003t0002g0209 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.740-463A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986882 | ||||||
| chr4:38986896
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0005g0187 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-477T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986896 | ||||||
| chr4:38986900
|
T | C | 3 | a0001c0001t0002g0184a0001c0001t0008g0342a0001c0001t0008g0377 | 3 | HG01884.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.740-481A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986900 | ||||||
| chr4:38986912
|
T | C | 1 | a0004c0005t0002g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.740-493A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986912 | ||||||
| chr4:38986967
|
G | A | 113 | a0001c0001t0001g0026a0001c0001t0001g0109a0001c0001t0001g0124others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.740-548C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986967 | ||||||
| chr4:38986976
|
CA | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.740-558delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38986976 | ||||||
| chr4:38987001
|
G | T | 41 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.740-582C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987001 | ||||||
| chr4:38987086
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.740-667G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987086 | ||||||
| chr4:38987196
|
T | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.740-777A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987196 | ||||||
| chr4:38987499
|
A | G | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.740-1080T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987499 | ||||||
| chr4:38987689
|
T | C | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(28): Show | 31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.739+1162A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987689 | ||||||
| chr4:38987845
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+1006T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987845 | ||||||
| chr4:38987928
|
T | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0185a0001c0001t0001g0324others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.739+923A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987928 | ||||||
| chr4:38987940
|
T | C | 3 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0013g0293 | 3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.739+911A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38987940 | ||||||
| chr4:38988063
|
C | T | 1 | a0002c0002t0003g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.739+788G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988063 | ||||||
| chr4:38988127
|
G | A | 23 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+724C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988127 | ||||||
| chr4:38988172
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(30): Show | 33 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.739+679G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988172 | ||||||
| chr4:38988178
|
T | C | 2 | a0002c0002t0001g0336a0002c0002t0003g0279 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.739+673A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988178 | ||||||
| chr4:38988187
|
C | G | 32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0140others(29): Show | 32 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.739+664G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988187 | ||||||
| chr4:38988320
|
C | T | 209 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.739+531G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988320 | ||||||
| chr4:38988372
|
C | T | 9 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(6): Show | 9 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+479G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988372 | ||||||
| chr4:38988416
|
C | G | 208 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.739+435G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988416 | ||||||
| chr4:38988434
|
GGCTGGTC others(1): Show |
G | 209 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.739+409_739+416del others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988434 | ||||||
| chr4:38988474
|
C | A | 19 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(16): Show | 20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.739+377G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988474 | ||||||
| chr4:38988509
|
G | A | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739+342C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988509 | ||||||
| chr4:38988512
|
ATGAGTCA others(12): Show |
A | 1 | a0001c0001t0004g0055 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.739+320_739+338del others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988512 | ||||||
| chr4:38988526
|
T | C | 208 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.739+325A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988526 | ||||||
| chr4:38988610
|
T | C | 177 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.739+241A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988610 | ||||||
| chr4:38988645
|
T | C | 177 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.739+206A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988645 | ||||||
| chr4:38988651
|
T | TACTC | 177 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.739+199_739+200ins others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988651 | ||||||
| chr4:38988684
|
T | C | 3 | a0004c0005t0001g0226a0004c0005t0003g0212a0004c0005t0005g0165 | 3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.739+167A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988684 | ||||||
| chr4:38988714
|
C | T | 177 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.739+137G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988714 | ||||||
| chr4:38988716
|
T | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.739+135A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988716 | ||||||
| chr4:38988763
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+88C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988763 | ||||||
| chr4:38988808
|
G | C | 1 | a0002c0002t0001g0350 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.739+43C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988808 | ||||||
| chr4:38988824
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.739+27G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 4/6 | chr4 | 38988824 | ||||||
| chr4:38989030
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0003g0132 | 2 | NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.620-60A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989030 | ||||||
| chr4:38989159
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0002g0347 | 2 | NA18964.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.620-189G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989159 | ||||||
| chr4:38989164
|
A | G | 18 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.620-194T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989164 | ||||||
| chr4:38989507
|
G | A | 3 | a0004c0005t0001g0226a0004c0005t0003g0212a0004c0005t0005g0165 | 3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.620-537C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989507 | ||||||
| chr4:38989621
|
A | G | 19 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(16): Show | 20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.620-651T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989621 | ||||||
| chr4:38989635
|
T | G | 279 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.620-665A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989635 | ||||||
| chr4:38989638
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(25): Show | 28 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.620-668T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989638 | ||||||
| chr4:38989641
|
A | T | 27 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(24): Show | 27 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.620-671T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989641 | ||||||
| chr4:38989669
|
A | G | 27 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0160others(24): Show | 27 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.620-699T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989669 | ||||||
| chr4:38989752
|
C | G | 1 | a0001c0001t0002g0343 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.620-782G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989752 | ||||||
| chr4:38989768
|
TTTTTA | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.620-803_620-799del others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989768 | ||||||
| chr4:38989770
|
T | TTTATTTT others(13): Show |
1 | a0001c0001t0003g0290 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.620-820_620-801dup others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989770 | ||||||
| chr4:38989770
|
TTTATTTT others(13): Show |
T | 1 | a0001c0001t0008g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.620-820_620-801del others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989770 | ||||||
| chr4:38989790
|
C | CTTATT | 3 | a0001c0001t0001g0171a0001c0001t0005g0187a0002c0002t0001g0365 | 3 | HG01361.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.620-825_620-821dup others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989790 | ||||||
| chr4:38989889
|
T | C | 281 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(278): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.620-919A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989889 | ||||||
| chr4:38989892
|
C | T | 1 | a0002c0002t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.620-922G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989892 | ||||||
| chr4:38989956
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0065a0001c0001t0004g0263 | 3 | HG01175.hp2 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.620-986C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989956 | ||||||
| chr4:38989987
|
G | T | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.620-1017C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38989987 | ||||||
| chr4:38990042
|
G | A | 1 | a0002c0002t0002g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.620-1072C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990042 | ||||||
| chr4:38990087
|
A | G | 1 | a0001c0001t0005g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.620-1117T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990087 | ||||||
| chr4:38990148
|
G | C | 233 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.620-1178C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990148 | ||||||
| chr4:38990238
|
C | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(28): Show | 31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.620-1268G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990238 | ||||||
| chr4:38990294
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.620-1324C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990294 | ||||||
| chr4:38990337
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.620-1367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990337 | ||||||
| chr4:38990357
|
A | G | 2 | a0001c0001t0002g0175a0001c0011t0001g0198 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.620-1387T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990357 | ||||||
| chr4:38990390
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0117 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.620-1420G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990390 | ||||||
| chr4:38990394
|
C | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.620-1424G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990394 | ||||||
| chr4:38990530
|
A | C | 1 | a0001c0001t0001g0202 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.620-1560T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990530 | ||||||
| chr4:38990531
|
A | G | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(226): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.620-1561T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990531 | ||||||
| chr4:38990556
|
A | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0026others(148): Show | 153 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.620-1586T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990556 | ||||||
| chr4:38990612
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.620-1642A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990612 | ||||||
| chr4:38990626
|
C | A | 60 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.620-1656G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990626 | ||||||
| chr4:38990628
|
C | T | 1 | a0001c0003t0002g0151 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.620-1658G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990628 | ||||||
| chr4:38990659
|
A | G | 237 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(234): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.620-1689T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990659 | ||||||
| chr4:38990679
|
A | C | 1 | a0001c0003t0004g0310 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.620-1709T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990679 | ||||||
| chr4:38990685
|
G | A | 237 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(234): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.620-1715C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990685 | ||||||
| chr4:38990745
|
G | C | 238 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(235): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.620-1775C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990745 | ||||||
| chr4:38990750
|
C | G | 238 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(235): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.620-1780G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990750 | ||||||
| chr4:38990774
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.620-1804G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990774 | ||||||
| chr4:38990791
|
G | T | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.620-1821C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990791 | ||||||
| chr4:38990820
|
T | A | 1 | a0001c0003t0004g0023 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.620-1850A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990820 | ||||||
| chr4:38990830
|
G | GT | 23 | a0001c0001t0001g0024a0001c0001t0001g0143a0001c0001t0001g0152others(20): Show | 23 | HG01175.hp1 HG01978.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.620-1861dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTC | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(30): Show | 33 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.620-1861_620-1860i others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTT | 17 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0162others(14): Show | 17 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.620-1864_620-1861d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTT | 12 | a0001c0001t0001g0188a0001c0001t0001g0222a0001c0001t0001g0323others(9): Show | 12 | HG01243.hp1 HG01433.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1865_620-1861d others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0040a0001c0001t0001g0309a0001c0001t0001g0316others(3): Show | 6 | HG02129.hp1 HG02165.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.620-1873_620-1861d others(15): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0276a0001c0001t0003g0311others(1): Show | 4 | HG00438.hp1 HG02145.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1874_620-1861d others(16): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0357a0001c0001t0002g0099a0001c0009t0001g0066 | 3 | NA19001.hp2 NA19074.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.620-1875_620-1861d others(17): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.620-1861_620-1860i others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0369others(1): Show | 4 | HG00544.hp1 NA18968.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-1876_620-1861d others(18): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(10): Show |
7 | a0001c0001t0001g0037a0001c0001t0001g0081a0001c0001t0001g0335others(4): Show | 7 | HG00609.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.620-1877_620-1861d others(19): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(11): Show |
6 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0044others(3): Show | 6 | HG01074.hp1 HG01361.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1878_620-1861d others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(12): Show |
9 | a0001c0001t0001g0120a0001c0001t0001g0138a0001c0001t0002g0070others(6): Show | 9 | HG00099.hp2 HG01952.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.620-1879_620-1861d others(21): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0001g0019 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.620-1881_620-1861d others(23): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990830
|
GT | G | 7 | a0001c0001t0001g0294a0001c0001t0002g0339a0001c0001t0005g0270others(4): Show | 7 | HG00597.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-1861delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990830 | ||||||
| chr4:38990831
|
T | TTTC | 107 | a0001c0001t0001g0026a0001c0001t0003g0067a0001c0001t0003g0132others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.620-1862_620-1861i others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990831 | ||||||
| chr4:38990835
|
T | TTTTTTTT others(11): Show |
17 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(14): Show | 18 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.620-1866_620-1865i others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990835 | ||||||
| chr4:38990841
|
T | TTGTTTTG others(11): Show |
1 | a0001c0001t0005g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.620-1872_620-1871i others(20): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990841 | ||||||
| chr4:38990886
|
T | A | 2 | a0001c0001t0002g0031a0001c0001t0005g0286 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.620-1916A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990886 | ||||||
| chr4:38990889
|
G | A | 209 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.620-1919C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990889 | ||||||
| chr4:38990902
|
C | T | 209 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.620-1932G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990902 | ||||||
| chr4:38990909
|
C | G | 4 | a0001c0001t0003g0178a0001c0001t0005g0167a0001c0001t0005g0177others(1): Show | 4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-1939G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990909 | ||||||
| chr4:38990927
|
G | A | 209 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.620-1957C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990927 | ||||||
| chr4:38990929
|
G | A | 6 | a0001c0001t0002g0180a0001c0001t0002g0192a0001c0001t0002g0225others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1959C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990929 | ||||||
| chr4:38990939
|
G | T | 210 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.620-1969C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990939 | ||||||
| chr4:38990959
|
G | A | 210 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.620-1989C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38990959 | ||||||
| chr4:38991084
|
C | G | 3 | a0001c0001t0001g0173a0001c0001t0002g0011a0001c0001t0005g0007 | 3 | HG02717.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.620-2114G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991084 | ||||||
| chr4:38991133
|
T | C | 200 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(197): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.620-2163A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991133 | ||||||
| chr4:38991206
|
C | CT | 178 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.620-2237dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991206 | ||||||
| chr4:38991206
|
C | CTT | 19 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(16): Show | 20 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.620-2238_620-2237d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991206 | ||||||
| chr4:38991212
|
C | T | 200 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(197): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.620-2242G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991212 | ||||||
| chr4:38991227
|
C | CT | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.620-2258dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991227 | ||||||
| chr4:38991227
|
CT | C | 8 | a0002c0002t0002g0125a0003c0004t0003g0016a0004c0005t0001g0226others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.620-2258delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991227 | ||||||
| chr4:38991381
|
T | C | 201 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.619+2357A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991381 | ||||||
| chr4:38991477
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.619+2261A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991477 | ||||||
| chr4:38991540
|
C | T | 2 | a0002c0002t0001g0259a0002c0002t0002g0256 | 2 | HG02738.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.619+2198G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991540 | ||||||
| chr4:38991564
|
C | T | 43 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.619+2174G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991564 | ||||||
| chr4:38991574
|
A | G | 159 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(156): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.619+2164T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991574 | ||||||
| chr4:38991674
|
AAC | A | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+2062_619+2063d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991674 | ||||||
| chr4:38991758
|
G | A | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+1980C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991758 | ||||||
| chr4:38991803
|
A | G | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+1935T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991803 | ||||||
| chr4:38991890
|
T | C | 1 | a0002c0002t0004g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.619+1848A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991890 | ||||||
| chr4:38991899
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.619+1839T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991899 | ||||||
| chr4:38991951
|
C | A | 14 | a0002c0002t0001g0022a0002c0002t0001g0063a0002c0002t0002g0002others(11): Show | 15 | HG02071.hp2 NA18747.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.619+1787G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38991951 | ||||||
| chr4:38992003
|
G | A | 154 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(151): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.619+1735C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992003 | ||||||
| chr4:38992005
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.619+1733C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992005 | ||||||
| chr4:38992032
|
C | A | 1 | a0002c0002t0002g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.619+1706G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992032 | ||||||
| chr4:38992064
|
G | A | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+1674C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992064 | ||||||
| chr4:38992168
|
G | A | 3 | a0002c0002t0001g0219a0002c0002t0003g0043a0002c0002t0003g0080 | 3 | HG02300.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.619+1570C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992168 | ||||||
| chr4:38992409
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.619+1329C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992409 | ||||||
| chr4:38992475
|
A | C | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+1263T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992475 | ||||||
| chr4:38992535
|
T | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.619+1203A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992535 | ||||||
| chr4:38992567
|
G | T | 177 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.619+1171C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992567 | ||||||
| chr4:38992611
|
G | C | 1 | a0001c0001t0008g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.619+1127C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992611 | ||||||
| chr4:38992665
|
CATATATA others(54): Show |
C | 2 | a0001c0001t0005g0190a0001c0001t0009g0189 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+1012_619+1072d others(63): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992665 | ||||||
| chr4:38992667
|
TATATATA others(61): Show |
T | 154 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(151): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.619+1003_619+1070d others(70): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992667 | ||||||
| chr4:38992679
|
ATATTATA others(62): Show |
A | 21 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(18): Show | 22 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.619+990_619+1058de others(70): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992679 | ||||||
| chr4:38992681
|
AT | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0085others(28): Show | 31 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.619+1056delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992681 | ||||||
| chr4:38992681
|
ATTATATA others(75): Show |
A | 4 | a0001c0001t0003g0178a0001c0001t0005g0167a0001c0001t0005g0177others(1): Show | 4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.619+975_619+1056de others(83): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992681 | ||||||
| chr4:38992682
|
T | TATATAA | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+1055_619+1056i others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | ||||||
| chr4:38992682
|
T | TTATATAA others(40): Show |
1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.619+1009_619+1055d others(49): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | ||||||
| chr4:38992682
|
T | TTATATAA others(47): Show |
1 | a0001c0003t0004g0310 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.619+1002_619+1055d others(56): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992682 | ||||||
| chr4:38992686
|
A | ATTAT | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+1051_619+1052i others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992686 | ||||||
| chr4:38992686
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.619+1052T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992686 | ||||||
| chr4:38992700
|
AAT | A | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.619+1036_619+1037d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992700 | ||||||
| chr4:38992701
|
A | ATATATAT others(2): Show |
25 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0085others(22): Show | 25 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.619+1028_619+1036d others(11): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992701 | ||||||
| chr4:38992702
|
T | TATATATA others(13): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0136 | 3 | HG02145.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.619+1035_619+1036i others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | ||||||
| chr4:38992702
|
T | TATATATA others(24): Show |
2 | a0001c0001t0001g0171a0001c0001t0005g0187 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.619+1035_619+1036i others(33): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | ||||||
| chr4:38992702
|
T | TATATATA others(79): Show |
1 | a0004c0005t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.619+1035_619+1036i others(88): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992702 | ||||||
| chr4:38992703
|
A | ATATATAT others(4): Show |
2 | a0004c0005t0001g0226a0004c0005t0003g0212 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.619+1034_619+1035i others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992703 | ||||||
| chr4:38992703
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.619+1035T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992703 | ||||||
| chr4:38992706
|
T | TATATATT others(29): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0368 | 2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.619+996_619+1031du others(37): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992706 | ||||||
| chr4:38992713
|
T | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(30): Show | 33 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.619+1025A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992713 | ||||||
| chr4:38992714
|
A | T | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.619+1024T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992714 | ||||||
| chr4:38992715
|
T | A | 2 | a0001c0001t0002g0339a0001c0001t0003g0098 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.619+1023A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992715 | ||||||
| chr4:38992724
|
A | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0129a0001c0001t0001g0152others(1): Show | 4 | HG00639.hp2 HG01175.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.619+1014T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992724 | ||||||
| chr4:38992747
|
AT | A | 112 | a0001c0001t0001g0026a0001c0001t0005g0190a0001c0001t0009g0189others(109): Show | 114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.619+990delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992747 | ||||||
| chr4:38992748
|
T | TA | 44 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.619+989_619+990ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992748 | ||||||
| chr4:38992748
|
TTA | T | 3 | a0004c0005t0001g0226a0004c0005t0003g0212a0004c0005t0005g0165 | 3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.619+988_619+989del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992748 | ||||||
| chr4:38992758
|
A | T | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.619+980T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992758 | ||||||
| chr4:38992760
|
A | T | 16 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0185others(13): Show | 16 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.619+978T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992760 | ||||||
| chr4:38992762
|
A | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0105a0001c0001t0001g0140others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.619+976T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992762 | ||||||
| chr4:38992762
|
AT | A | 22 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(19): Show | 22 | HG00423.hp1 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.619+975delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992762 | ||||||
| chr4:38992764
|
T | A | 136 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0029others(133): Show | 138 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.619+974A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992764 | ||||||
| chr4:38992766
|
T | A | 11 | a0001c0001t0001g0026a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.619+972A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992766 | ||||||
| chr4:38992772
|
G | T | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+966C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992772 | ||||||
| chr4:38992831
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619+907C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992831 | ||||||
| chr4:38992847
|
C | T | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+891G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992847 | ||||||
| chr4:38992892
|
C | G | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+846G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992892 | ||||||
| chr4:38992912
|
C | A | 1 | a0002c0002t0003g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619+826G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992912 | ||||||
| chr4:38992921
|
C | T | 2 | a0001c0001t0002g0269a0001c0001t0007g0062 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.619+817G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992921 | ||||||
| chr4:38992929
|
T | A | 43 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.619+809A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992929 | ||||||
| chr4:38992951
|
C | T | 1 | a0001c0003t0003g0332 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.619+787G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38992951 | ||||||
| chr4:38993013
|
A | G | 178 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.619+725T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993013 | ||||||
| chr4:38993050
|
C | T | 2 | a0001c0001t0005g0190a0001c0001t0009g0189 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+688G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993050 | ||||||
| chr4:38993146
|
A | G | 2 | a0001c0001t0005g0190a0001c0001t0009g0189 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.619+592T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993146 | ||||||
| chr4:38993255
|
C | A | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+483G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993255 | ||||||
| chr4:38993258
|
C | T | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+480G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993258 | ||||||
| chr4:38993261
|
C | T | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.619+477G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993261 | ||||||
| chr4:38993344
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.619+394A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993344 | ||||||
| chr4:38993399
|
T | C | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.619+339A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993399 | ||||||
| chr4:38993461
|
TA | T | 156 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.619+276delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993461 | ||||||
| chr4:38993690
|
A | G | 158 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.619+48T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993690 | ||||||
| chr4:38993698
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.619+40G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 3/6 | chr4 | 38993698 | ||||||
| chr4:38994108
|
G | A | 5 | a0001c0003t0001g0205a0001c0003t0002g0206a0001c0003t0002g0209others(2): Show | 5 | HG00280.hp2 HG01070.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-110C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994108 | ||||||
| chr4:38994291
|
A | G | 160 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.359-293T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994291 | ||||||
| chr4:38994363
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.359-365C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994363 | ||||||
| chr4:38994441
|
A | G | 114 | a0001c0001t0001g0026a0002c0002t0001g0012a0002c0002t0001g0022others(111): Show | 116 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.359-443T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994441 | ||||||
| chr4:38994509
|
A | C | 186 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.359-511T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994509 | ||||||
| chr4:38994567
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-569T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994567 | ||||||
| chr4:38994614
|
G | A | 164 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.359-616C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994614 | ||||||
| chr4:38994672
|
A | G | 186 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.359-674T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994672 | ||||||
| chr4:38994679
|
C | T | 164 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.359-681G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994679 | ||||||
| chr4:38994684
|
C | T | 164 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.359-686G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994684 | ||||||
| chr4:38994721
|
G | A | 20 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(17): Show | 21 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-723C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994721 | ||||||
| chr4:38994764
|
A | G | 50 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.359-766T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994764 | ||||||
| chr4:38994808
|
C | T | 1 | a0001c0001t0005g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.359-810G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994808 | ||||||
| chr4:38994821
|
G | A | 20 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(17): Show | 21 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-823C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994821 | ||||||
| chr4:38994852
|
C | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-854G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994852 | ||||||
| chr4:38994873
|
C | G | 50 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.359-875G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994873 | ||||||
| chr4:38994952
|
A | C | 3 | a0004c0005t0002g0170a0004c0005t0002g0174a0004c0005t0005g0165 | 3 | HG02622.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.359-954T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38994952 | ||||||
| chr4:38995054
|
G | A | 50 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.359-1056C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995054 | ||||||
| chr4:38995142
|
G | A | 3 | a0001c0001t0001g0288a0001c0001t0001g0368a0001c0001t0002g0289 | 3 | HG01255.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.359-1144C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995142 | ||||||
| chr4:38995159
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.359-1161G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995159 | ||||||
| chr4:38995222
|
A | G | 164 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0026others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.359-1224T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995222 | ||||||
| chr4:38995246
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-1248C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995246 | ||||||
| chr4:38995282
|
G | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-1284C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995282 | ||||||
| chr4:38995408
|
C | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.359-1410G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995408 | ||||||
| chr4:38995534
|
A | G | 163 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-1536T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995534 | ||||||
| chr4:38995604
|
A | C | 163 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.359-1606T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995604 | ||||||
| chr4:38995609
|
G | A | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.359-1611C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995609 | ||||||
| chr4:38995656
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-1658T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995656 | ||||||
| chr4:38995677
|
T | C | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.359-1679A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995677 | ||||||
| chr4:38995688
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.359-1690G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995688 | ||||||
| chr4:38995850
|
G | T | 3 | a0004c0005t0001g0226a0004c0005t0003g0212a0004c0005t0005g0165 | 3 | HG02055.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.359-1852C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995850 | ||||||
| chr4:38995852
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.359-1854A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995852 | ||||||
| chr4:38995873
|
A | T | 1 | a0001c0003t0003g0332 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.359-1875T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995873 | ||||||
| chr4:38995971
|
T | A | 70 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.359-1973A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38995971 | ||||||
| chr4:38996237
|
C | T | 1 | a0002c0002t0002g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.359-2239G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996237 | ||||||
| chr4:38996262
|
G | GA | 70 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.359-2265dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996262 | ||||||
| chr4:38996262
|
GA | G | 10 | a0001c0001t0001g0109a0001c0001t0001g0171a0001c0001t0002g0192others(7): Show | 10 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-2265delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996262 | ||||||
| chr4:38996275
|
AAG | A | 105 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.359-2279_359-2278d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996275 | ||||||
| chr4:38996276
|
A | AC | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-2279_359-2278i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996276 | ||||||
| chr4:38996276
|
AG | A | 7 | a0002c0002t0001g0148a0002c0002t0002g0116a0002c0002t0003g0325others(4): Show | 7 | HG02559.hp2 HG04184.hp2 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-2279delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996276 | ||||||
| chr4:38996324
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.358+2316G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996324 | ||||||
| chr4:38996389
|
C | T | 113 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+2251G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996389 | ||||||
| chr4:38996406
|
C | CA | 17 | a0001c0001t0002g0099a0001c0001t0003g0028a0002c0002t0001g0012others(14): Show | 17 | HG01433.hp1 HG02135.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.358+2233dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | ||||||
| chr4:38996406
|
C | CAA | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+2232_358+2233d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | ||||||
| chr4:38996406
|
CA | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0171others(15): Show | 18 | HG01975.hp1 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.358+2233delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996406 | ||||||
| chr4:38996497
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.358+2143T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996497 | ||||||
| chr4:38996597
|
C | T | 1 | a0002c0002t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.358+2043G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996597 | ||||||
| chr4:38996604
|
G | A | 113 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+2036C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996604 | ||||||
| chr4:38996672
|
C | A | 5 | a0001c0001t0002g0192a0001c0001t0002g0225a0001c0001t0003g0195others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+1968G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996672 | ||||||
| chr4:38996829
|
G | A | 45 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(42): Show | 45 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+1811C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996829 | ||||||
| chr4:38996972
|
A | G | 1 | a0002c0002t0004g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.358+1668T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38996972 | ||||||
| chr4:38997068
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358+1572T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997068 | ||||||
| chr4:38997077
|
C | T | 1 | a0001c0001t0004g0095 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.358+1563G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997077 | ||||||
| chr4:38997086
|
G | C | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+1554C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997086 | ||||||
| chr4:38997153
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+1487A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997153 | ||||||
| chr4:38997347
|
C | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1293G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997347 | ||||||
| chr4:38997412
|
A | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.358+1228T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997412 | ||||||
| chr4:38997439
|
TA | T | 5 | a0001c0001t0002g0192a0001c0001t0002g0225a0001c0001t0003g0195others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+1200delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997439 | ||||||
| chr4:38997542
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358+1098T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997542 | ||||||
| chr4:38997646
|
G | T | 5 | a0001c0001t0001g0139a0001c0003t0001g0331a0001c0003t0001g0361others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+994C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997646 | ||||||
| chr4:38997828
|
A | G | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+812T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997828 | ||||||
| chr4:38997937
|
A | C | 1 | a0004c0005t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.358+703T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997937 | ||||||
| chr4:38997958
|
T | A | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+682A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997958 | ||||||
| chr4:38997968
|
G | A | 70 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.358+672C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38997968 | ||||||
| chr4:38998103
|
A | G | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+537T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998103 | ||||||
| chr4:38998174
|
G | A | 201 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.358+466C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998174 | ||||||
| chr4:38998267
|
A | G | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+373T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998267 | ||||||
| chr4:38998271
|
G | T | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+369C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998271 | ||||||
| chr4:38998310
|
G | A | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+330C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998310 | ||||||
| chr4:38998352
|
T | C | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+288A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998352 | ||||||
| chr4:38998412
|
C | T | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+228G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998412 | ||||||
| chr4:38998523
|
A | G | 118 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.358+117T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998523 | ||||||
| chr4:38998543
|
C | CAAA | 113 | a0002c0002t0001g0012a0002c0002t0001g0022a0002c0002t0001g0030others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.358+94_358+96dupTT others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998543 | ||||||
| chr4:38998543
|
CA | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+96delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998543 | ||||||
| chr4:38998571
|
T | A | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358+69A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 2/6 | chr4 | 38998571 | ||||||
| chr4:38998936
|
C | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0112a0001c0001t0004g0095 | 3 | HG00609.hp1 NA18953.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.89-27G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38998936 | ||||||
| chr4:38998949
|
C | T | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-40G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38998949 | ||||||
| chr4:38999022
|
G | T | 70 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.89-113C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999022 | ||||||
| chr4:38999029
|
A | G | 123 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-120T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999029 | ||||||
| chr4:38999110
|
AT | A | 168 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(165): Show | 168 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.89-202delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | ||||||
| chr4:38999110
|
ATT | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0376a0001c0001t0002g0147others(3): Show | 6 | HG00423.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-203_89-202delAA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | ||||||
| chr4:38999110
|
ATTTTTT | A | 112 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(109): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.89-207_89-202delAA others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | ||||||
| chr4:38999110
|
ATTTTTTT others(3): Show |
A | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-211_89-202delAA others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999110 | ||||||
| chr4:38999111
|
T | TTTA | 70 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0039others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.89-203_89-202insTA others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999111 | ||||||
| chr4:38999114
|
T | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0358a0001c0001t0002g0289others(2): Show | 5 | HG01361.hp1 HG02165.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-205A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999114 | ||||||
| chr4:38999114
|
T | TA | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-206_89-205insT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999114 | ||||||
| chr4:38999115
|
T | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.89-206A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999115 | ||||||
| chr4:38999116
|
T | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0376a0001c0001t0002g0147others(3): Show | 6 | HG00280.hp2 HG00423.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-207A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999116 | ||||||
| chr4:38999118
|
T | A | 13 | a0001c0001t0001g0021a0001c0001t0001g0160a0001c0001t0001g0162others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.89-209A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999118 | ||||||
| chr4:38999119
|
T | A | 119 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0086others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-210A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999119 | ||||||
| chr4:38999120
|
T | A | 146 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0039others(143): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.89-211A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999120 | ||||||
| chr4:38999123
|
T | A | 39 | a0001c0001t0001g0053a0001c0001t0001g0109a0001c0001t0001g0124others(36): Show | 40 | HG00099.hp1 HG00544.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-214A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999123 | ||||||
| chr4:38999124
|
T | A | 8 | a0002c0002t0001g0262a0002c0002t0001g0266a0002c0002t0001g0291others(5): Show | 8 | HG00621.hp2 HG00673.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-215A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999124 | ||||||
| chr4:38999125
|
T | A | 4 | a0001c0001t0003g0178a0001c0001t0005g0167a0001c0001t0005g0177others(1): Show | 4 | HG02970.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-216A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999125 | ||||||
| chr4:38999127
|
T | A | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-218A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999127 | ||||||
| chr4:38999128
|
T | A | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-219A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999128 | ||||||
| chr4:38999174
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-265A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999174 | ||||||
| chr4:38999180
|
A | G | 1 | a0001c0001t0004g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.89-271T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999180 | ||||||
| chr4:38999190
|
T | C | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-281A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999190 | ||||||
| chr4:38999456
|
CCTTAGAT others(1): Show |
C | 42 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-555_89-548delAA others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999456 | ||||||
| chr4:38999698
|
T | A | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-789A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999698 | ||||||
| chr4:38999987
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.89-1078G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999987 | ||||||
| chr4:38999990
|
A | C | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1081T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 38999990 | ||||||
| chr4:39000047
|
A | C | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1138T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000047 | ||||||
| chr4:39000094
|
CA | C | 5 | a0002c0002t0001g0101a0002c0002t0001g0145a0002c0002t0002g0059others(2): Show | 5 | HG00741.hp2 HG01192.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1186delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000094 | ||||||
| chr4:39000101
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89-1192G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000101 | ||||||
| chr4:39000105
|
C | T | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1196G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000105 | ||||||
| chr4:39000120
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.89-1211C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000120 | ||||||
| chr4:39000137
|
T | C | 2 | a0002c0002t0002g0135a0002c0002t0002g0315 | 2 | HG00609.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.89-1228A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000137 | ||||||
| chr4:39000253
|
G | A | 1 | a0001c0001t0006g0314 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.89-1344C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000253 | ||||||
| chr4:39000289
|
T | G | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1380A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000289 | ||||||
| chr4:39000327
|
A | G | 1 | a0001c0003t0006g0321 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.89-1418T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000327 | ||||||
| chr4:39000338
|
A | G | 123 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1429T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000338 | ||||||
| chr4:39000379
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.89-1470C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000379 | ||||||
| chr4:39000468
|
C | T | 8 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1559G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000468 | ||||||
| chr4:39000563
|
T | C | 2 | a0002c0002t0001g0240a0002c0002t0001g0241 | 2 | NA19056.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.89-1654A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000563 | ||||||
| chr4:39000565
|
G | A | 70 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.89-1656C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000565 | ||||||
| chr4:39000570
|
T | C | 123 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1661A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000570 | ||||||
| chr4:39000613
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0004g0014a0001c0001t0006g0015others(2): Show | 5 | HG02015.hp2 NA18612.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1704C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000613 | ||||||
| chr4:39000629
|
G | A | 1 | a0001c0001t0002g0320 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.89-1720C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000629 | ||||||
| chr4:39000650
|
G | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.89-1741C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000650 | ||||||
| chr4:39000652
|
T | C | 123 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1743A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000652 | ||||||
| chr4:39000685
|
G | A | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-1776C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000685 | ||||||
| chr4:39000757
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-1848C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000757 | ||||||
| chr4:39000763
|
T | C | 123 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.89-1854A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000763 | ||||||
| chr4:39000814
|
G | C | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1905C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000814 | ||||||
| chr4:39000880
|
C | G | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-1971G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39000880 | ||||||
| chr4:39001013
|
A | G | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2104T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001013 | ||||||
| chr4:39001128
|
C | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0171others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2219G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001128 | ||||||
| chr4:39001128
|
C | T | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2219G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001128 | ||||||
| chr4:39001179
|
G | A | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-2270C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001179 | ||||||
| chr4:39001214
|
C | CA | 31 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0087others(28): Show | 31 | HG00423.hp1 HG01081.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2306dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | ||||||
| chr4:39001214
|
C | CAA | 68 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0039others(65): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.89-2307_89-2306dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | ||||||
| chr4:39001214
|
C | CAAA | 9 | a0001c0001t0001g0202a0001c0001t0002g0099a0001c0001t0003g0178others(6): Show | 9 | HG02970.hp1 HG03130.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-2308_89-2306dup others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | ||||||
| chr4:39001214
|
CA | C | 102 | a0001c0001t0001g0139a0001c0001t0005g0164a0001c0003t0002g0209others(99): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.89-2306delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001214 | ||||||
| chr4:39001280
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0004g0217 | 2 | NA18961.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.89-2371T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001280 | ||||||
| chr4:39001451
|
A | C | 1 | a0001c0001t0008g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-2542T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001451 | ||||||
| chr4:39001538
|
C | CT | 115 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.89-2630dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001538 | ||||||
| chr4:39001541
|
C | CT | 48 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.89-2633dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001541 | ||||||
| chr4:39001541
|
C | T | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2632G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001541 | ||||||
| chr4:39001544
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0003g0132 | 2 | NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.89-2635A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001544 | ||||||
| chr4:39001578
|
A | T | 2 | a0001c0001t0001g0143a0001c0001t0002g0065 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.89-2669T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001578 | ||||||
| chr4:39001630
|
C | T | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2721G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001630 | ||||||
| chr4:39001634
|
A | G | 50 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.89-2725T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001634 | ||||||
| chr4:39001659
|
A | G | 42 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-2750T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001659 | ||||||
| chr4:39001712
|
T | C | 120 | a0001c0001t0001g0139a0001c0001t0005g0270a0001c0001t0011g0182others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.89-2803A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001712 | ||||||
| chr4:39001728
|
G | A | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2819C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001728 | ||||||
| chr4:39001733
|
T | C | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-2824A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001733 | ||||||
| chr4:39001740
|
C | G | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2831G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001740 | ||||||
| chr4:39001899
|
T | C | 117 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(114): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.89-2990A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001899 | ||||||
| chr4:39001905
|
C | T | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-2996G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001905 | ||||||
| chr4:39001929
|
C | A | 1 | a0004c0005t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-3020G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001929 | ||||||
| chr4:39001969
|
A | G | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3060T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001969 | ||||||
| chr4:39001989
|
T | C | 188 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.89-3080A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39001989 | ||||||
| chr4:39002018
|
A | C | 190 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-3109T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002018 | ||||||
| chr4:39002170
|
C | T | 5 | a0001c0001t0001g0260a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG00544.hp2 HG03490.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3261G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002170 | ||||||
| chr4:39002219
|
C | T | 6 | a0004c0005t0001g0118a0004c0005t0001g0226a0004c0005t0002g0170others(3): Show | 6 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002219 | ||||||
| chr4:39002220
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.89-3311C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002220 | ||||||
| chr4:39002266
|
A | G | 1 | a0002c0002t0002g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.89-3357T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002266 | ||||||
| chr4:39002276
|
C | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3367G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002276 | ||||||
| chr4:39002382
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.89-3473G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002382 | ||||||
| chr4:39002383
|
G | A | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3474C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002383 | ||||||
| chr4:39002449
|
G | C | 5 | a0004c0005t0001g0226a0004c0005t0002g0170a0004c0005t0002g0174others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3540C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002449 | ||||||
| chr4:39002458
|
T | C | 1 | a0004c0005t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-3549A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002458 | ||||||
| chr4:39002473
|
C | T | 191 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(188): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.89-3564G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002473 | ||||||
| chr4:39002585
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0060others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3676C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002585 | ||||||
| chr4:39002597
|
A | C | 190 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-3688T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002597 | ||||||
| chr4:39002683
|
G | A | 10 | a0002c0002t0001g0234a0002c0002t0002g0141a0004c0005t0001g0226others(7): Show | 10 | HG02055.hp1 HG02148.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-3774C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002683 | ||||||
| chr4:39002706
|
A | C | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3797T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002706 | ||||||
| chr4:39002727
|
T | C | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-3818A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002727 | ||||||
| chr4:39002800
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-3891G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002800 | ||||||
| chr4:39002885
|
G | C | 121 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.89-3976C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002885 | ||||||
| chr4:39002885
|
G | T | 2 | a0001c0001t0005g0270a0001c0001t0011g0182 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.89-3976C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002885 | ||||||
| chr4:39002939
|
C | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4030G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002939 | ||||||
| chr4:39002939
|
C | T | 190 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-4030G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002939 | ||||||
| chr4:39002943
|
T | C | 1 | a0001c0001t0003g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.89-4034A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002943 | ||||||
| chr4:39002966
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0002g0159 | 2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.89-4057A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39002966 | ||||||
| chr4:39003054
|
G | A | 118 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.89-4145C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003054 | ||||||
| chr4:39003129
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.89-4220C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003129 | ||||||
| chr4:39003181
|
G | T | 209 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.89-4272C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003181 | ||||||
| chr4:39003191
|
T | A | 1 | a0002c0002t0001g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.89-4282A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003191 | ||||||
| chr4:39003386
|
G | A | 1 | a0001c0001t0004g0354 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.89-4477C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003386 | ||||||
| chr4:39003391
|
G | A | 120 | a0001c0001t0001g0139a0001c0001t0005g0270a0001c0001t0011g0182others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.89-4482C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003391 | ||||||
| chr4:39003469
|
G | A | 3 | a0006c0008t0001g0370a0006c0008t0003g0338a0006c0008t0006g0285 | 3 | HG02647.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-4560C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003469 | ||||||
| chr4:39003522
|
C | T | 117 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(114): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.89-4613G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003522 | ||||||
| chr4:39003576
|
C | T | 3 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0013g0293 | 3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-4667G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003576 | ||||||
| chr4:39003585
|
C | A | 1 | a0002c0002t0001g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.89-4676G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003585 | ||||||
| chr4:39003652
|
TA | T | 223 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0037others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.89-4744delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003652 | ||||||
| chr4:39003728
|
G | A | 206 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.89-4819C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003728 | ||||||
| chr4:39003733
|
T | G | 2 | a0001c0003t0001g0331a0001c0003t0001g0361 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.89-4824A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003733 | ||||||
| chr4:39003740
|
A | T | 2 | a0002c0002t0002g0215a0002c0002t0005g0381 | 2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.89-4831T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003740 | ||||||
| chr4:39003865
|
A | G | 1 | a0001c0003t0004g0023 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.89-4956T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003865 | ||||||
| chr4:39003879
|
A | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0292others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4970T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003879 | ||||||
| chr4:39003981
|
C | T | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.89-5072G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39003981 | ||||||
| chr4:39004614
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-5705C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004614 | ||||||
| chr4:39004634
|
T | A | 1 | a0002c0002t0001g0291 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.89-5725A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004634 | ||||||
| chr4:39004838
|
A | G | 3 | a0001c0003t0002g0006a0001c0003t0003g0097a0001c0003t0004g0023 | 3 | NA18940.hp1 NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.89-5929T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004838 | ||||||
| chr4:39004925
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.89-6016G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004925 | ||||||
| chr4:39004995
|
T | C | 1 | a0001c0001t0008g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-6086A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39004995 | ||||||
| chr4:39005146
|
C | T | 209 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.89-6237G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005146 | ||||||
| chr4:39005149
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.89-6240T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005149 | ||||||
| chr4:39005172
|
G | C | 125 | a0001c0001t0001g0139a0002c0002t0001g0012a0002c0002t0001g0022others(122): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-6263C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005172 | ||||||
| chr4:39005210
|
G | A | 10 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0181others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-6301C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005210 | ||||||
| chr4:39005224
|
G | A | 17 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0127others(14): Show | 18 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-6315C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005224 | ||||||
| chr4:39005385
|
C | A | 1 | a0002c0002t0001g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.89-6476G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005385 | ||||||
| chr4:39005532
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0002g0065 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.89-6623T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005532 | ||||||
| chr4:39005546
|
G | A | 125 | a0001c0001t0001g0139a0001c0001t0001g0292a0001c0001t0002g0192others(122): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-6637C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005546 | ||||||
| chr4:39005551
|
G | T | 3 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0013g0293 | 3 | HG02257.hp2 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-6642C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005551 | ||||||
| chr4:39005561
|
AG | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.89-6653delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005561 | ||||||
| chr4:39005562
|
G | A | 168 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(165): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.89-6653C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005562 | ||||||
| chr4:39005597
|
AC | A | 6 | a0001c0001t0003g0178a0001c0001t0005g0167a0001c0001t0005g0177others(3): Show | 6 | HG02970.hp1 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-6689delG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005597 | ||||||
| chr4:39005891
|
G | A | 52 | a0001c0001t0001g0173a0001c0001t0001g0287a0001c0001t0002g0011others(49): Show | 52 | HG00733.hp2 HG01891.hp2 HG01934.hp2 others(49): Show |
intron_variant | MODIFIER | c.89-6982C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005891 | ||||||
| chr4:39005895
|
A | G | 1 | a0001c0003t0004g0023 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.89-6986T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005895 | ||||||
| chr4:39005902
|
C | A | 2 | a0001c0001t0001g0248a0001c0001t0004g0247 | 2 | NA19009.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.89-6993G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005902 | ||||||
| chr4:39005964
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.89-7055G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005964 | ||||||
| chr4:39005981
|
T | C | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.89-7072A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39005981 | ||||||
| chr4:39006033
|
T | C | 1 | a0001c0003t0002g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.89-7124A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006033 | ||||||
| chr4:39006047
|
C | T | 4 | a0004c0005t0001g0226a0004c0005t0003g0212a0006c0008t0003g0338others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-7138G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006047 | ||||||
| chr4:39006159
|
G | C | 1 | a0001c0001t0005g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89-7250C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006159 | ||||||
| chr4:39006162
|
C | T | 1 | a0001c0001t0005g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-7253G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006162 | ||||||
| chr4:39006372
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.89-7463G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006372 | ||||||
| chr4:39006472
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-7563C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006472 | ||||||
| chr4:39006485
|
T | C | 16 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0001t0001g0172others(13): Show | 16 | HG00099.hp1 HG01168.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-7576A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006485 | ||||||
| chr4:39006495
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.89-7586T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006495 | ||||||
| chr4:39006630
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.89-7721C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006630 | ||||||
| chr4:39006633
|
C | A | 3 | a0001c0001t0002g0031a0001c0001t0005g0270a0001c0001t0005g0286 | 3 | HG02615.hp1 HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7724G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006633 | ||||||
| chr4:39006657
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.89-7748G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006657 | ||||||
| chr4:39006812
|
G | A | 1 | a0001c0011t0001g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-7903C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006812 | ||||||
| chr4:39006881
|
C | T | 2 | a0001c0001t0002g0031a0001c0001t0005g0286 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7972G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006881 | ||||||
| chr4:39006962
|
A | C | 3 | a0001c0001t0001g0288a0001c0001t0002g0289a0001c0001t0005g0267 | 3 | HG02145.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.89-8053T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39006962 | ||||||
| chr4:39007031
|
C | A | 104 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0061others(101): Show | 104 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.89-8122G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007031 | ||||||
| chr4:39007066
|
C | T | 275 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.89-8157G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007066 | ||||||
| chr4:39007113
|
T | C | 4 | a0001c0001t0008g0377a0006c0008t0001g0370a0006c0008t0003g0338others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-8204A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007113 | ||||||
| chr4:39007173
|
G | A | 152 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0053others(149): Show | 152 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.89-8264C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007173 | ||||||
| chr4:39007185
|
C | G | 129 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(126): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.89-8276G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007185 | ||||||
| chr4:39007201
|
T | C | 5 | a0001c0001t0005g0164a0002c0002t0001g0168a0002c0002t0001g0169others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-8292A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007201 | ||||||
| chr4:39007236
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.89-8327C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007236 | ||||||
| chr4:39007345
|
G | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0002g0269others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8436C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007345 | ||||||
| chr4:39007415
|
T | TTTTATTT others(1): Show |
50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0160others(47): Show | 50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-8514_89-8507dup others(8): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007415 | ||||||
| chr4:39007701
|
C | A | 11 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0222others(8): Show | 11 | HG01255.hp2 HG02572.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-8792G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007701 | ||||||
| chr4:39007720
|
G | T | 2 | a0004c0005t0002g0170a0004c0005t0002g0174 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.89-8811C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007720 | ||||||
| chr4:39007811
|
T | A | 3 | a0001c0001t0001g0362a0001c0001t0002g0122a0002c0002t0002g0089 | 3 | NA19058.hp1 NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.89-8902A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007811 | ||||||
| chr4:39007897
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0160others(47): Show | 50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-8988A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007897 | ||||||
| chr4:39007945
|
T | A | 27 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-9036A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39007945 | ||||||
| chr4:39008133
|
T | G | 1 | a0001c0001t0004g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.89-9224A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008133 | ||||||
| chr4:39008219
|
C | T | 1 | a0001c0001t0005g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-9310G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008219 | ||||||
| chr4:39008233
|
T | G | 1 | a0001c0001t0004g0355 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.89-9324A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008233 | ||||||
| chr4:39008348
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0002g0112a0001c0001t0004g0014others(22): Show | 27 | HG00609.hp1 HG02071.hp2 NA18747.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-9439G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008348 | ||||||
| chr4:39008360
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-9451A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008360 | ||||||
| chr4:39008602
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0007g0062 | 3 | HG01167.hp2 HG01169.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.89-9693C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008602 | ||||||
| chr4:39008625
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-9716A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008625 | ||||||
| chr4:39008632
|
C | T | 38 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0158others(35): Show | 38 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-9723G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008632 | ||||||
| chr4:39008756
|
A | G | 2 | a0001c0001t0005g0190a0004c0005t0001g0118 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.89-9847T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008756 | ||||||
| chr4:39008790
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0016g0106 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.89-9881G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39008790 | ||||||
| chr4:39009258
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0160others(47): Show | 50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-10349T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009258 | ||||||
| chr4:39009351
|
A | T | 325 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.89-10442T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009351 | ||||||
| chr4:39009475
|
G | A | 2 | a0004c0005t0002g0170a0004c0005t0002g0174 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.89-10566C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009475 | ||||||
| chr4:39009490
|
A | T | 1 | a0001c0001t0003g0378 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.89-10581T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009490 | ||||||
| chr4:39009669
|
C | T | 1 | a0001c0001t0005g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.89-10760G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009669 | ||||||
| chr4:39009696
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0160others(47): Show | 50 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.89-10787T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009696 | ||||||
| chr4:39009862
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.89-10953T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39009862 | ||||||
| chr4:39010207
|
T | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0297others(6): Show | 9 | HG01192.hp1 HG01261.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-11298A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010207 | ||||||
| chr4:39010220
|
A | G | 1 | a0002c0002t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.89-11311T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010220 | ||||||
| chr4:39010289
|
G | A | 15 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0001g0202others(12): Show | 15 | HG00099.hp1 HG01168.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.89-11380C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010289 | ||||||
| chr4:39010887
|
C | T | 324 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.89-11978G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39010887 | ||||||
| chr4:39011010
|
T | C | 41 | a0001c0001t0001g0053a0001c0001t0001g0129a0001c0001t0001g0157others(38): Show | 41 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-12101A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011010 | ||||||
| chr4:39011277
|
G | A | 27 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-12368C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011277 | ||||||
| chr4:39011354
|
C | A | 3 | a0001c0001t0001g0163a0001c0001t0002g0225a0004c0005t0005g0165 | 3 | HG02622.hp1 HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.89-12445G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011354 | ||||||
| chr4:39011368
|
G | A | 14 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(11): Show | 14 | HG01255.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-12459C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011368 | ||||||
| chr4:39011399
|
A | G | 4 | a0001c0001t0008g0377a0006c0008t0001g0370a0006c0008t0003g0338others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-12490T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011399 | ||||||
| chr4:39011449
|
T | TA | 27 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-12541dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011449 | ||||||
| chr4:39011644
|
A | T | 309 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.89-12735T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011644 | ||||||
| chr4:39011646
|
G | C | 268 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.89-12737C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011646 | ||||||
| chr4:39011666
|
C | A | 1 | a0001c0001t0002g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-12757G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011666 | ||||||
| chr4:39011704
|
C | T | 1 | a0001c0001t0005g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-12795G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011704 | ||||||
| chr4:39011705
|
G | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-12796C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011705 | ||||||
| chr4:39011756
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0003g0051 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.89-12847C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011756 | ||||||
| chr4:39011899
|
G | T | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-12990C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39011899 | ||||||
| chr4:39012025
|
G | T | 5 | a0001c0001t0005g0286a0001c0001t0008g0377a0006c0008t0001g0370others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-13116C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012025 | ||||||
| chr4:39012029
|
G | A | 1 | a0002c0002t0002g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-13120C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012029 | ||||||
| chr4:39012113
|
G | A | 1 | a0001c0001t0005g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-13204C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012113 | ||||||
| chr4:39012123
|
A | G | 2 | a0001c0001t0005g0190a0004c0005t0001g0118 | 2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.89-13214T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012123 | ||||||
| chr4:39012169
|
T | A | 1 | a0002c0002t0004g0103 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.89-13260A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012169 | ||||||
| chr4:39012172
|
A | T | 1 | a0002c0002t0004g0103 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.89-13263T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012172 | ||||||
| chr4:39012193
|
A | G | 5 | a0002c0002t0001g0240a0002c0002t0001g0241a0002c0002t0001g0262others(2): Show | 5 | HG00621.hp2 NA19000.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-13284T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012193 | ||||||
| chr4:39012275
|
A | G | 193 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(190): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.89-13366T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012275 | ||||||
| chr4:39012624
|
G | C | 186 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.89-13715C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012624 | ||||||
| chr4:39012673
|
G | A | 1 | a0001c0001t0003g0132 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.89-13764C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012673 | ||||||
| chr4:39012714
|
C | T | 186 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.89-13805G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012714 | ||||||
| chr4:39012738
|
G | A | 1 | a0002c0002t0002g0252 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.89-13829C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012738 | ||||||
| chr4:39012948
|
A | G | 1 | a0001c0001t0003g0146 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.89-14039T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012948 | ||||||
| chr4:39012995
|
G | T | 38 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0158others(35): Show | 38 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-14086C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39012995 | ||||||
| chr4:39013098
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.89-14189G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013098 | ||||||
| chr4:39013133
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.89-14224A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013133 | ||||||
| chr4:39013307
|
CA | C | 127 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0053others(124): Show | 127 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.89-14399delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013307 | ||||||
| chr4:39013320
|
AG | A | 4 | a0001c0001t0008g0377a0006c0008t0001g0370a0006c0008t0003g0338others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-14412delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013320 | ||||||
| chr4:39013321
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-14412C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013321 | ||||||
| chr4:39013325
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-14416C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013325 | ||||||
| chr4:39013362
|
T | A | 1 | a0001c0001t0001g0358 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.89-14453A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013362 | ||||||
| chr4:39013373
|
GTTTA | G | 89 | a0001c0001t0001g0053a0001c0001t0001g0081a0001c0001t0001g0086others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.89-14468_89-14465d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013373
|
GTTTATTT others(1): Show |
G | 166 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(163): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.89-14472_89-14465d others(10): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013373
|
GTTTATTT others(5): Show |
G | 77 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0094others(74): Show | 77 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.89-14476_89-14465d others(14): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013373
|
GTTTATTT others(9): Show |
G | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(30): Show | 33 | HG01192.hp1 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-14480_89-14465d others(18): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013373
|
GTTTATTT others(13): Show |
G | 6 | a0001c0001t0002g0184a0001c0001t0005g0007a0001c0001t0008g0377others(3): Show | 6 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-14484_89-14465d others(22): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013373
|
GTTTATTT others(17): Show |
G | 1 | a0001c0001t0004g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.89-14488_89-14465d others(26): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013373 | ||||||
| chr4:39013481
|
A | AC | 197 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(194): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.89-14573dupG | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013481 | ||||||
| chr4:39013589
|
C | T | 4 | a0001c0001t0008g0377a0006c0008t0001g0370a0006c0008t0003g0338others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-14680G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013589 | ||||||
| chr4:39013652
|
G | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-14743C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013652 | ||||||
| chr4:39013990
|
C | G | 2 | a0001c0001t0001g0288a0001c0001t0002g0289 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.89-15081G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39013990 | ||||||
| chr4:39014146
|
A | C | 27 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(24): Show | 27 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-15237T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014146 | ||||||
| chr4:39014225
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0002g0345 | 2 | HG01168.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.89-15316G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014225 | ||||||
| chr4:39014380
|
A | C | 1 | a0001c0001t0001g0335 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-15471T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014380 | ||||||
| chr4:39014455
|
T | C | 293 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.89-15546A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014455 | ||||||
| chr4:39014570
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.89-15661G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014570 | ||||||
| chr4:39014591
|
T | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-15682A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014591 | ||||||
| chr4:39014650
|
CG | C | 11 | a0001c0001t0001g0216a0001c0001t0001g0372a0001c0001t0001g0375others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-15742delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014650 | ||||||
| chr4:39014655
|
G | C | 5 | a0002c0002t0001g0034a0002c0002t0001g0057a0002c0002t0003g0058others(2): Show | 5 | NA18939.hp1 NA18948.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-15746C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014655 | ||||||
| chr4:39014757
|
CA | C | 114 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0053others(111): Show | 114 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.89-15849delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014757 | ||||||
| chr4:39014757
|
CAA | C | 184 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(181): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.89-15850_89-15849d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39014757 | ||||||
| chr4:39015171
|
G | T | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-16262C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015171 | ||||||
| chr4:39015272
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.89-16363C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015272 | ||||||
| chr4:39015408
|
T | C | 2 | a0001c0001t0003g0220a0002c0002t0001g0219 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.89-16499A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015408 | ||||||
| chr4:39015575
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88+16651G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015575 | ||||||
| chr4:39015580
|
G | C | 1 | a0002c0002t0003g0325 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.88+16646C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015580 | ||||||
| chr4:39015632
|
A | T | 2 | a0001c0001t0001g0276a0002c0007t0003g0344 | 2 | NA18966.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.88+16594T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015632 | ||||||
| chr4:39015914
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+16312G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39015914 | ||||||
| chr4:39016223
|
A | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0160others(46): Show | 49 | HG01109.hp2 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.88+16003T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016223 | ||||||
| chr4:39016263
|
C | T | 7 | a0001c0001t0001g0372a0001c0001t0001g0375a0001c0001t0001g0376others(4): Show | 7 | HG02647.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+15963G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016263 | ||||||
| chr4:39016298
|
G | T | 102 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.88+15928C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016298 | ||||||
| chr4:39016371
|
T | TA | 62 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0001g0152others(59): Show | 62 | HG00323.hp1 HG00423.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.88+15854dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016371 | ||||||
| chr4:39016383
|
AAAG | A | 18 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0207others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+15840_88+15842d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016383 | ||||||
| chr4:39016385
|
AG | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0011others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+15840delC | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016385 | ||||||
| chr4:39016386
|
G | A | 186 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(183): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.88+15840C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016386 | ||||||
| chr4:39016387
|
A | AC | 7 | a0001c0001t0001g0150a0001c0001t0001g0216a0001c0001t0003g0220others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+15838_88+15839i others(3): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016387 | ||||||
| chr4:39016387
|
A | C | 55 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0140others(52): Show | 55 | HG00280.hp1 HG00639.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+15839T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016387 | ||||||
| chr4:39016752
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0011others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+15474A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016752 | ||||||
| chr4:39016771
|
T | C | 1 | a0002c0002t0002g0363 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.88+15455A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016771 | ||||||
| chr4:39016840
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+15386G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016840 | ||||||
| chr4:39016842
|
G | A | 44 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0171others(41): Show | 44 | HG01109.hp2 HG01168.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.88+15384C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39016842 | ||||||
| chr4:39017018
|
A | G | 2 | a0002c0002t0001g0030a0002c0002t0001g0049 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.88+15208T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017018 | ||||||
| chr4:39017171
|
C | CTT | 8 | a0001c0001t0001g0102a0001c0001t0001g0152a0001c0001t0001g0162others(5): Show | 8 | HG01168.hp2 HG01175.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+15053_88+15054d others(4): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | ||||||
| chr4:39017171
|
C | CTTT | 189 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.88+15052_88+15054d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | ||||||
| chr4:39017171
|
C | CTTTT | 29 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0138others(26): Show | 29 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.88+15051_88+15054d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | ||||||
| chr4:39017171
|
CT | C | 39 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0248others(36): Show | 39 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.88+15054delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017171 | ||||||
| chr4:39017202
|
T | C | 3 | a0001c0001t0001g0216a0004c0005t0001g0226a0004c0005t0003g0212 | 3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15024A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017202 | ||||||
| chr4:39017203
|
C | G | 3 | a0001c0001t0001g0216a0004c0005t0001g0226a0004c0005t0003g0212 | 3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15023G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017203 | ||||||
| chr4:39017204
|
T | A | 3 | a0001c0001t0001g0216a0004c0005t0001g0226a0004c0005t0003g0212 | 3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15022A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017204 | ||||||
| chr4:39017205
|
C | G | 3 | a0001c0001t0001g0216a0004c0005t0001g0226a0004c0005t0003g0212 | 3 | HG02055.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+15021G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017205 | ||||||
| chr4:39017205
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+15021G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017205 | ||||||
| chr4:39017206
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0003g0265a0004c0005t0001g0226others(1): Show | 4 | HG02055.hp1 HG02602.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+15020C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017206 | ||||||
| chr4:39017299
|
C | T | 5 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(2): Show | 5 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+14927G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017299 | ||||||
| chr4:39017324
|
G | A | 9 | a0001c0001t0001g0188a0001c0001t0002g0192a0001c0001t0003g0195others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+14902C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017324 | ||||||
| chr4:39017332
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.88+14894C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017332 | ||||||
| chr4:39017340
|
AATTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0328 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.88+14875_88+14885d others(13): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017340 | ||||||
| chr4:39017713
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0002g0147 | 2 | NA19005.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.88+14513A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017713 | ||||||
| chr4:39017963
|
A | T | 5 | a0001c0001t0001g0133a0001c0001t0003g0130a0001c0001t0003g0132others(2): Show | 5 | HG02015.hp1 NA18951.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14263T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39017963 | ||||||
| chr4:39018032
|
G | C | 5 | a0001c0001t0001g0216a0001c0001t0004g0214a0001c0001t0004g0221others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14194C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018032 | ||||||
| chr4:39018257
|
T | C | 57 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.88+13969A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018257 | ||||||
| chr4:39018267
|
C | A | 7 | a0001c0001t0001g0372a0001c0001t0001g0375a0001c0001t0001g0376others(4): Show | 7 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+13959G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018267 | ||||||
| chr4:39018292
|
G | T | 223 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.88+13934C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018292 | ||||||
| chr4:39018294
|
T | C | 223 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.88+13932A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018294 | ||||||
| chr4:39018340
|
T | C | 2 | a0001c0001t0003g0220a0002c0002t0001g0219 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.88+13886A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018340 | ||||||
| chr4:39018574
|
T | G | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(154): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.88+13652A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018574 | ||||||
| chr4:39018629
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.88+13597G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018629 | ||||||
| chr4:39018677
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+13549T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018677 | ||||||
| chr4:39018709
|
C | A | 2 | a0004c0005t0001g0226a0004c0005t0003g0212 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+13517G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018709 | ||||||
| chr4:39018805
|
T | G | 222 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.88+13421A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018805 | ||||||
| chr4:39018842
|
G | T | 24 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(21): Show | 24 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.88+13384C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018842 | ||||||
| chr4:39018855
|
T | C | 2 | a0004c0005t0001g0226a0004c0005t0003g0212 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.88+13371A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018855 | ||||||
| chr4:39018893
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+13333G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018893 | ||||||
| chr4:39018978
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+13248C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018978 | ||||||
| chr4:39018996
|
G | A | 1 | a0002c0002t0001g0266 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.88+13230C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39018996 | ||||||
| chr4:39019023
|
AAAAAC | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0188others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+13198_88+13202d others(7): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019023 | ||||||
| chr4:39019024
|
AAAAC | A | 46 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.88+13198_88+13201d others(6): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019024 | ||||||
| chr4:39019025
|
AAAC | A | 16 | a0001c0001t0001g0202a0001c0001t0002g0180a0001c0001t0002g0184others(13): Show | 16 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+13198_88+13200d others(5): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019025 | ||||||
| chr4:39019026
|
AACAAAAC | A | 147 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.88+13193_88+13199d others(9): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019026 | ||||||
| chr4:39019033
|
C | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0158others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.88+13193G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | ||||||
| chr4:39019033
|
C | CA | 7 | a0001c0001t0001g0366a0001c0001t0002g0208a0001c0001t0004g0364others(4): Show | 7 | HG00621.hp1 HG01361.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+13192dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | ||||||
| chr4:39019033
|
C | G | 2 | a0001c0001t0002g0147a0001c0003t0004g0023 | 2 | NA18940.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.88+13193G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019033 | ||||||
| chr4:39019034
|
A | G | 143 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.88+13192T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019034 | ||||||
| chr4:39019035
|
A | G | 1 | a0002c0002t0006g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.88+13191T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019035 | ||||||
| chr4:39019038
|
A | C | 15 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0372others(12): Show | 15 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.88+13188T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019038 | ||||||
| chr4:39019039
|
A | C | 2 | a0001c0001t0001g0288a0001c0001t0002g0289 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88+13187T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019039 | ||||||
| chr4:39019041
|
A | C | 2 | a0004c0005t0002g0170a0004c0005t0002g0174 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.88+13185T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019041 | ||||||
| chr4:39019050
|
C | A | 4 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(1): Show | 4 | HG02723.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+13176G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019050 | ||||||
| chr4:39019133
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+13093C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019133 | ||||||
| chr4:39019271
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0004g0014a0001c0001t0006g0015others(1): Show | 4 | NA18943.hp1 NA18972.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+12955A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019271 | ||||||
| chr4:39019299
|
T | C | 3 | a0001c0001t0001g0105a0001c0001t0016g0106a0002c0002t0001g0104 | 3 | HG00323.hp2 HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.88+12927A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019299 | ||||||
| chr4:39019405
|
T | C | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+12821A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019405 | ||||||
| chr4:39019497
|
C | T | 4 | a0001c0001t0002g0208a0001c0003t0001g0205a0001c0003t0002g0206others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+12729G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019497 | ||||||
| chr4:39019700
|
T | C | 156 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(153): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.88+12526A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019700 | ||||||
| chr4:39019920
|
T | C | 1 | a0004c0005t0002g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+12306A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39019920 | ||||||
| chr4:39020025
|
A | G | 5 | a0001c0001t0001g0216a0001c0001t0004g0214a0001c0001t0004g0221others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+12201T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020025 | ||||||
| chr4:39020125
|
A | T | 274 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.88+12101T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020125 | ||||||
| chr4:39020142
|
T | C | 1 | a0001c0001t0005g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+12084A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020142 | ||||||
| chr4:39020226
|
T | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0002g0011others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+12000A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020226 | ||||||
| chr4:39020290
|
C | T | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.88+11936G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020290 | ||||||
| chr4:39020359
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.88+11867G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020359 | ||||||
| chr4:39020461
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.88+11765G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020461 | ||||||
| chr4:39020490
|
C | A | 8 | a0001c0001t0001g0372a0001c0001t0001g0375a0001c0001t0001g0376others(5): Show | 8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+11736G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020490 | ||||||
| chr4:39020648
|
C | A | 2 | a0001c0001t0002g0379a0001c0001t0005g0380 | 2 | HG01167.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.88+11578G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020648 | ||||||
| chr4:39020659
|
C | A | 11 | a0001c0001t0002g0112a0002c0002t0001g0022a0002c0002t0002g0002others(8): Show | 12 | HG00609.hp1 HG02071.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+11567G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020659 | ||||||
| chr4:39020675
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+11551C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020675 | ||||||
| chr4:39020705
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.88+11521T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020705 | ||||||
| chr4:39020895
|
T | C | 217 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.88+11331A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020895 | ||||||
| chr4:39020913
|
C | T | 3 | a0001c0001t0004g0214a0001c0001t0004g0221a0002c0002t0002g0215 | 3 | HG02258.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88+11313G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020913 | ||||||
| chr4:39020920
|
G | A | 1 | a0001c0001t0006g0015 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.88+11306C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39020920 | ||||||
| chr4:39021009
|
A | G | 1 | a0002c0002t0003g0382 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.88+11217T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021009 | ||||||
| chr4:39021059
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.88+11167G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021059 | ||||||
| chr4:39021075
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+11151A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021075 | ||||||
| chr4:39021139
|
A | T | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+11087T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021139 | ||||||
| chr4:39021232
|
G | A | 221 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.88+10994C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021232 | ||||||
| chr4:39021394
|
C | CA | 268 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.88+10831dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021394 | ||||||
| chr4:39021412
|
T | A | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+10814A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021412 | ||||||
| chr4:39021416
|
A | T | 1 | a0001c0001t0005g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+10810T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021416 | ||||||
| chr4:39021436
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.88+10790A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021436 | ||||||
| chr4:39021592
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 6 | NA18957.hp1 NA18961.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+10634C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021592 | ||||||
| chr4:39021827
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+10399G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021827 | ||||||
| chr4:39021946
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+10280G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021946 | ||||||
| chr4:39021982
|
C | T | 1 | a0001c0001t0004g0295 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+10244G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39021982 | ||||||
| chr4:39022079
|
T | C | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(154): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.88+10147A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022079 | ||||||
| chr4:39022093
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.88+10133A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022093 | ||||||
| chr4:39022200
|
T | C | 4 | a0002c0002t0001g0259a0002c0002t0002g0256a0002c0002t0004g0257others(1): Show | 4 | HG02738.hp2 NA18942.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10026A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022200 | ||||||
| chr4:39022372
|
C | G | 227 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.88+9854G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022372 | ||||||
| chr4:39022901
|
GA | G | 4 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0008g0342others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9324delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022901 | ||||||
| chr4:39022911
|
C | G | 4 | a0001c0001t0001g0292a0001c0001t0002g0343a0001c0001t0008g0342others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9315G>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39022911 | ||||||
| chr4:39023068
|
A | T | 1 | a0002c0002t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+9158T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023068 | ||||||
| chr4:39023353
|
A | G | 99 | a0001c0001t0001g0129a0001c0001t0001g0160a0001c0001t0001g0162others(96): Show | 99 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.88+8873T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023353 | ||||||
| chr4:39023401
|
A | G | 4 | a0001c0001t0005g0164a0002c0002t0001g0168a0002c0002t0001g0169others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+8825T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023401 | ||||||
| chr4:39023766
|
A | G | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(154): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.88+8460T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023766 | ||||||
| chr4:39023851
|
T | C | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+8375A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023851 | ||||||
| chr4:39023885
|
C | A | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+8341G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39023885 | ||||||
| chr4:39024180
|
C | T | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+8046G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024180 | ||||||
| chr4:39024224
|
T | C | 272 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.88+8002A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024224 | ||||||
| chr4:39024334
|
C | A | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7892G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024334 | ||||||
| chr4:39024397
|
C | T | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7829G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024397 | ||||||
| chr4:39024432
|
A | T | 8 | a0001c0001t0001g0372a0001c0001t0001g0375a0001c0001t0001g0376others(5): Show | 8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+7794T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024432 | ||||||
| chr4:39024721
|
A | G | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+7505T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39024721 | ||||||
| chr4:39025076
|
C | T | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+7150G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025076 | ||||||
| chr4:39025113
|
C | A | 2 | a0001c0001t0001g0158a0001c0001t0002g0159 | 2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.88+7113G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025113 | ||||||
| chr4:39025138
|
C | T | 1 | a0001c0001t0005g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.88+7088G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025138 | ||||||
| chr4:39025206
|
A | G | 376 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(373): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.88+7020T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025206 | ||||||
| chr4:39025210
|
G | C | 59 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.88+7016C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025210 | ||||||
| chr4:39025250
|
C | A | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+6976G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025250 | ||||||
| chr4:39025264
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+6962G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025264 | ||||||
| chr4:39025315
|
T | C | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+6911A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025315 | ||||||
| chr4:39025345
|
C | CA | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(143): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.88+6880dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | ||||||
| chr4:39025345
|
C | CAA | 18 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0120others(15): Show | 18 | HG01123.hp1 HG01361.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.88+6879_88+6880dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | ||||||
| chr4:39025345
|
CA | C | 46 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 46 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.88+6880delT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025345 | ||||||
| chr4:39025462
|
T | C | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(154): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.88+6764A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025462 | ||||||
| chr4:39025521
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88+6705C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025521 | ||||||
| chr4:39025617
|
G | A | 2 | a0002c0002t0002g0383a0002c0002t0003g0382 | 2 | HG00673.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.88+6609C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025617 | ||||||
| chr4:39025656
|
G | A | 2 | a0001c0001t0003g0003a0002c0002t0001g0134 | 3 | HG01069.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.88+6570C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025656 | ||||||
| chr4:39025656
|
G | C | 1 | a0001c0001t0011g0182 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.88+6570C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025656 | ||||||
| chr4:39025657
|
G | T | 1 | a0001c0001t0004g0153 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.88+6569C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025657 | ||||||
| chr4:39025684
|
T | G | 5 | a0001c0001t0001g0216a0001c0001t0004g0214a0001c0001t0004g0221others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+6542A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025684 | ||||||
| chr4:39025718
|
T | C | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+6508A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025718 | ||||||
| chr4:39025815
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0029others(6): Show | 9 | HG01123.hp1 HG01433.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6411G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39025815 | ||||||
| chr4:39026053
|
A | C | 1 | a0001c0001t0002g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.88+6173T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026053 | ||||||
| chr4:39026081
|
T | G | 1 | a0001c0001t0001g0369 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.88+6145A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026081 | ||||||
| chr4:39026128
|
T | C | 1 | a0001c0001t0002g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88+6098A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026128 | ||||||
| chr4:39026358
|
T | A | 2 | a0001c0001t0001g0216a0001c0001t0005g0267 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.88+5868A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026358 | ||||||
| chr4:39026365
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88+5861T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026365 | ||||||
| chr4:39026369
|
A | T | 2 | a0001c0001t0001g0288a0001c0001t0002g0289 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88+5857T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026369 | ||||||
| chr4:39026377
|
A | AG | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+5848_88+5849ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026377 | ||||||
| chr4:39026378
|
A | C | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+5848T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026378 | ||||||
| chr4:39026570
|
T | C | 50 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0152others(47): Show | 50 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.88+5656A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026570 | ||||||
| chr4:39026612
|
A | G | 2 | a0001c0001t0002g0340a0002c0002t0003g0341 | 2 | HG02135.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.88+5614T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026612 | ||||||
| chr4:39026698
|
G | A | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+5528C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026698 | ||||||
| chr4:39026787
|
C | T | 2 | a0001c0001t0003g0220a0002c0002t0001g0219 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.88+5439G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026787 | ||||||
| chr4:39026798
|
G | A | 43 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(40): Show | 43 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.88+5428C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026798 | ||||||
| chr4:39026820
|
G | A | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+5406C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39026820 | ||||||
| chr4:39027004
|
T | G | 8 | a0001c0001t0001g0372a0001c0001t0001g0375a0001c0001t0001g0376others(5): Show | 8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+5222A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027004 | ||||||
| chr4:39027025
|
C | T | 1 | a0001c0003t0004g0023 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.88+5201G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027025 | ||||||
| chr4:39027211
|
T | C | 1 | a0002c0002t0002g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88+5015A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027211 | ||||||
| chr4:39027436
|
G | T | 48 | a0001c0001t0001g0133a0001c0001t0001g0231a0001c0001t0001g0232others(45): Show | 48 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+4790C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027436 | ||||||
| chr4:39027548
|
T | G | 1 | a0002c0002t0003g0367 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.88+4678A>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027548 | ||||||
| chr4:39027551
|
C | CT | 22 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0287others(19): Show | 22 | HG00733.hp1 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.88+4674dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | ||||||
| chr4:39027551
|
CT | C | 238 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(235): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.88+4674delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | ||||||
| chr4:39027551
|
CTT | C | 17 | a0001c0001t0001g0127a0001c0001t0001g0154a0001c0001t0001g0160others(14): Show | 17 | HG01169.hp1 HG01255.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+4673_88+4674del others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027551 | ||||||
| chr4:39027758
|
C | CT | 13 | a0001c0001t0001g0216a0001c0001t0001g0222a0001c0001t0002g0223others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+4467dupA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027758 | ||||||
| chr4:39027758
|
C | CTT | 151 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(148): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.88+4466_88+4467dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027758 | ||||||
| chr4:39027761
|
T | TC | 55 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.88+4464_88+4465ins others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027761 | ||||||
| chr4:39027762
|
T | C | 2 | a0001c0001t0004g0211a0001c0003t0002g0209 | 2 | HG01169.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.88+4464A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027762 | ||||||
| chr4:39027764
|
T | C | 1 | a0001c0001t0001g0369 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.88+4462A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027764 | ||||||
| chr4:39027849
|
T | C | 49 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0231others(46): Show | 49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+4377A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39027849 | ||||||
| chr4:39028016
|
C | CA | 49 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0231others(46): Show | 49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+4209dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028016 | ||||||
| chr4:39028020
|
G | A | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+4206C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028020 | ||||||
| chr4:39028077
|
G | A | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+4149C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028077 | ||||||
| chr4:39028153
|
T | A | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+4073A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028153 | ||||||
| chr4:39028306
|
A | G | 1 | a0006c0008t0001g0370 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.88+3920T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028306 | ||||||
| chr4:39028563
|
A | G | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+3663T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028563 | ||||||
| chr4:39028820
|
A | G | 50 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0231others(47): Show | 50 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.88+3406T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028820 | ||||||
| chr4:39028872
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.88+3354T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39028872 | ||||||
| chr4:39029058
|
A | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG00323.hp1 HG01243.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+3168T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029058 | ||||||
| chr4:39029157
|
T | C | 49 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0231others(46): Show | 49 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+3069A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029157 | ||||||
| chr4:39029420
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0333 | 2 | HG02273.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.88+2806T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029420 | ||||||
| chr4:39029456
|
TAAGAACT others(275): Show |
T | 279 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.88+2488_88+2769del | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029456 | ||||||
| chr4:39029524
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.88+2702G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029524 | ||||||
| chr4:39029545
|
T | C | 1 | a0001c0003t0003g0332 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.88+2681A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029545 | ||||||
| chr4:39029596
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.88+2630G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029596 | ||||||
| chr4:39029713
|
C | CA | 38 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(35): Show | 38 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.88+2512dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029713 | ||||||
| chr4:39029757
|
A | C | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+2469T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029757 | ||||||
| chr4:39029764
|
C | A | 5 | a0001c0001t0001g0207a0001c0001t0002g0208a0001c0003t0001g0205others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+2462G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029764 | ||||||
| chr4:39029972
|
T | C | 47 | a0001c0001t0001g0133a0001c0001t0001g0231a0001c0001t0001g0232others(44): Show | 47 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.88+2254A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39029972 | ||||||
| chr4:39030179
|
T | TA | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+2046dupT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030179 | ||||||
| chr4:39030179
|
T | TAA | 8 | a0001c0001t0002g0264a0001c0001t0003g0220a0001c0001t0003g0265others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+2045_88+2046dup others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030179 | ||||||
| chr4:39030193
|
C | A | 42 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+2033G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030193 | ||||||
| chr4:39030222
|
C | T | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+2004G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030222 | ||||||
| chr4:39030289
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0007g0161others(1): Show | 4 | HG01255.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1937C>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030289 | ||||||
| chr4:39030359
|
C | T | 42 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+1867G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030359 | ||||||
| chr4:39030481
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0002g0223a0001c0001t0002g0225others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+1745G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030481 | ||||||
| chr4:39030565
|
A | T | 1 | a0002c0002t0005g0381 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88+1661T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030565 | ||||||
| chr4:39030723
|
G | A | 59 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.88+1503C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030723 | ||||||
| chr4:39030747
|
C | A | 42 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+1479G>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030747 | ||||||
| chr4:39030952
|
G | C | 1 | a0001c0001t0004g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.88+1274C>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39030952 | ||||||
| chr4:39031403
|
T | A | 1 | a0001c0001t0004g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+823A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031403 | ||||||
| chr4:39031469
|
T | C | 1 | a0001c0001t0004g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+757A>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031469 | ||||||
| chr4:39031572
|
A | G | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0162others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+654T>C | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031572 | ||||||
| chr4:39031761
|
G | A | 2 | a0001c0001t0002g0379a0001c0001t0005g0380 | 2 | HG01167.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.88+465C>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031761 | ||||||
| chr4:39031782
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0004g0014a0001c0001t0006g0015others(1): Show | 4 | NA18943.hp1 NA18972.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+444G>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031782 | ||||||
| chr4:39031875
|
T | A | 2 | a0001c0001t0003g0003a0002c0002t0001g0134 | 3 | HG01069.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.88+351A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031875 | ||||||
| chr4:39031887
|
AAAAT | A | 25 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(22): Show | 25 | HG01168.hp1 HG01255.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.88+335_88+338delAT others(2): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031887 | ||||||
| chr4:39031888
|
AAAT | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0158others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.88+335_88+337delAT others(1): Show |
TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031888 | ||||||
| chr4:39031889
|
AAT | A | 183 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(180): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.88+335_88+336delAT | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031889 | ||||||
| chr4:39031890
|
AT | A | 24 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(21): Show | 24 | HG01175.hp1 HG01346.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.88+335delA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031890 | ||||||
| chr4:39031891
|
T | A | 2 | a0001c0001t0001g0157a0002c0002t0005g0381 | 2 | HG03195.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.88+335A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031891 | ||||||
| chr4:39031894
|
A | T | 2 | a0001c0001t0002g0269a0001c0001t0005g0270 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.88+332T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031894 | ||||||
| chr4:39031898
|
T | A | 271 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.88+328A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031898 | ||||||
| chr4:39031902
|
A | C | 2 | a0001c0001t0001g0158a0001c0001t0002g0159 | 2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.88+324T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031902 | ||||||
| chr4:39031904
|
A | C | 1 | a0001c0003t0002g0006 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.88+322T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031904 | ||||||
| chr4:39031905
|
A | C | 270 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.88+321T>G | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031905 | ||||||
| chr4:39031913
|
A | AT | 158 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.88+312_88+313insA | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39031913 | ||||||
| chr4:39032117
|
T | A | 2 | a0002c0002t0002g0383a0002c0002t0003g0382 | 2 | HG00673.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.88+109A>T | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39032117 | ||||||
| chr4:39032186
|
A | T | 1 | a0002c0002t0004g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.88+40T>A | TMEM156 | ENSG00000121895.8 | transcript | ENST00000381938.4 | protein_coding | 1/6 | chr4 | 39032186 |