Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3626 |
|---|---|
| ensemblid | ENSG00000175189.4 |
| hgncid | 6068 |
| symbol | INHBC |
| name | inhibin subunit beta C |
| refseq_nuc | NM_005538.4 |
| refseq_prot | NP_005529.1 |
| ensembl_nuc | ENST00000309668.3 |
| ensembl_prot | ENSP00000308716.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 57434784 |
| end | 57452062 |
| strand | + |
| ver | v1.2 |
| region | chr12:57434784-57452062 |
| region5000 | chr12:57429784-57457062 |
| regionname0 | INHBC_chr12_57434784_57452062 |
| regionname5000 | INHBC_chr12_57429784_57457062 |
| 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 | 352 | 344 | 75 | 49 | 169 | 10 | 39 | 132 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0002 | 0/0 | 352 | 48 | 10 | 19 | 12 | 2 | 5 | 9 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0003 | 0/0 | 352 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0004 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0005 | 0/0 | 352 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1059 | 344 | 75 | 49 | 169 | 10 | 39 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| c0002 | 0/0 | 1059 | 48 | 10 | 19 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| c0003 | 0/0 | 1059 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| c0004 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| c0005 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2144 | 173 | 19 | 30 | 92 | 6 | 25 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0002 | 1/0 | 2144 | 145 | 38 | 17 | 71 | 4 | 14 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0003 | 0/0 | 2144 | 47 | 10 | 18 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0004 | 0/0 | 2144 | 9 | 9 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0005 | 0/0 | 2144 | 4 | 4 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0006 | 0/0 | 2144 | 3 | 2 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0007 | 0/0 | 2144 | 3 | 3 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0008 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0009 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0010 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0011 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0012 | 0/0 | 2144 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0013 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0014 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0015 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0016 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0017 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| t0018 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0007 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1059 | 344 | 75 | 49 | 169 | 10 | 39 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0002c0002 | 0/0 | 1059 | 48 | 10 | 19 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0003c0003 | 0/0 | 1059 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0004c0005 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0005c0004 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3202 | 173 | 19 | 30 | 92 | 6 | 25 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0002 | 1/0 | 3202 | 144 | 37 | 17 | 71 | 4 | 14 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0004 | 0/0 | 3202 | 9 | 9 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0005 | 0/0 | 3202 | 4 | 4 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0006 | 0/0 | 3202 | 3 | 2 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0007 | 0/0 | 3202 | 3 | 3 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0011 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0012 | 0/0 | 3202 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0013 | 0/0 | 3202 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0014 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0015 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0016 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0017 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0001c0001t0018 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0002c0002t0003 | 0/0 | 3202 | 47 | 10 | 18 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0002c0002t0009 | 0/0 | 3202 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0003c0003t0008 | 0/0 | 3189 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0004c0005t0010 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| a0005c0004t0002 | 0/0 | 3202 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | copy fasta | chr12 | 57429784 | 57457062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0007 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0011g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0013g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0014g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0016g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0018g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0003c0003t0008g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0003c0003t0008g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0004c0005t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0005c0004t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0311 | EUR | GBR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | FIN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0245 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0268 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0265 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0254 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01081 | hp2 | a0002 | c0002 | t0009 | g0255 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0246 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0259 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0351 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0239 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0269 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0257 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0278 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0367 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0276 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0014 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0243 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0371 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0256 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0258 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0275 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02004 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0264 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02071 | hp1 | a0001 | c0001 | t0018 | g0235 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02080 | hp1 | a0001 | c0001 | t0016 | g0221 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0267 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0366 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0274 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0147 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0270 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0013 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0266 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0279 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02965 | hp1 | a0003 | c0003 | t0008 | g0373 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0252 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0248 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0013 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0273 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0249 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0263 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0357 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0250 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0345 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0280 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0329 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0260 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0271 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18957 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0253 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0261 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18972 | hp2 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18974 | hp1 | a0004 | c0005 | t0010 | g0228 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0277 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18987 | hp1 | a0001 | c0001 | t0011 | g0289 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19056 | hp1 | a0001 | c0001 | t0014 | g0365 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0272 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | ASW | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | ASW | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0362 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | GIH | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0209 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0247 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG06807 | hp1 | a0003 | c0003 | t0008 | g0372 | AFR | USA | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | USA | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA21309 | hp1 | a0005 | c0004 | t0002 | g0319 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0007 | REF | REF | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57434980
|
C | G | 1 | a0004 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.94C>G | p.Pro32Ala | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 197/3202 | 94/1059 | 32/352 | chr12 | 57434980 | ||
| chr12:57434983
|
A | C | 1 | a0004 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.97A>C | p.Thr33Pro | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 200/3202 | 97/1059 | 33/352 | chr12 | 57434983 | ||
| chr12:57434984
|
C | A | 1 | a0004 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.98C>A | p.Thr33Asn | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 201/3202 | 98/1059 | 33/352 | chr12 | 57434984 | ||
| chr12:57449459
|
A | C | 1 | a0003 | 2 | HG02965.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.496A>C | p.Thr166Pro | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 599/3202 | 496/1059 | 166/352 | chr12 | 57449459 | ||
| chr12:57449862
|
A | G | 1 | a0005 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.899A>G | p.Asn300Ser | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1002/3202 | 899/1059 | 300/352 | chr12 | 57449862 | ||
| chr12:57449928
|
G | A | 1 | a0002 | 48 | HG00408.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
missense_variant | MODERATE | c.965G>A | p.Arg322Gln | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1068/3202 | 965/1059 | 322/352 | chr12 | 57449928 |
| 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 |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57434815
|
C | T | 1 | a0001c0001t0007 | 3 | HG02572.hp1 HG02809.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-72C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 72 | chr12 | 57434815 | |||||
| chr12:57434819
|
G | A | 1 | a0002c0002t0009 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-68G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 68 | chr12 | 57434819 | |||||
| chr12:57434857
|
T | G | 1 | a0004c0005t0010 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/2 | 30 | chr12 | 57434857 | |||||
| chr12:57450242
|
ATAGTCCA others(6): Show |
A | 1 | a0003c0003t0008 | 2 | HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*237_*249delTCCATC others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 237 | INFO_REALIGN_3_PRIME | chr12 | 57450242 | ||||
| chr12:57450266
|
C | T | 2 | a0002c0002t0003a0002c0002t0009 | 48 | HG00408.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 244 | chr12 | 57450266 | |||||
| chr12:57450302
|
A | G | 1 | a0001c0001t0018 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 280 | chr12 | 57450302 | |||||
| chr12:57450491
|
G | C | 1 | a0001c0001t0005 | 4 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*469G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 469 | chr12 | 57450491 | |||||
| chr12:57450504
|
C | A | 1 | a0001c0001t0011 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 482 | chr12 | 57450504 | |||||
| chr12:57450509
|
T | A | 1 | a0001c0001t0011 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*487T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 487 | chr12 | 57450509 | |||||
| chr12:57450567
|
T | G | 1 | a0001c0001t0012 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 545 | chr12 | 57450567 | |||||
| chr12:57450723
|
C | T | 1 | a0001c0001t0017 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 701 | chr12 | 57450723 | |||||
| chr12:57450929
|
T | A | 1 | a0001c0001t0013 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 907 | chr12 | 57450929 | |||||
| chr12:57450947
|
A | G | 1 | a0001c0001t0006 | 3 | HG01109.hp1 HG02897.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*925A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 925 | chr12 | 57450947 | |||||
| chr12:57451146
|
G | A | 1 | a0001c0001t0004 | 9 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1124 | chr12 | 57451146 | |||||
| chr12:57451380
|
C | A | 1 | a0001c0001t0014 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1358 | chr12 | 57451380 | |||||
| chr12:57451789
|
A | T | 1 | a0001c0001t0011 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1767 | chr12 | 57451789 | |||||
| chr12:57451817
|
C | T | 1 | a0001c0001t0016 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1795 | chr12 | 57451817 | |||||
| chr12:57451923
|
G | A | 5 | a0001c0001t0001a0001c0001t0007a0001c0001t0015others(2): Show | 179 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1901G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1901 | chr12 | 57451923 | |||||
| chr12:57451923
|
G | T | 1 | a0003c0003t0008 | 2 | HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1901G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 1901 | chr12 | 57451923 | |||||
| chr12:57452022
|
A | G | 1 | a0001c0001t0015 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 2/2 | 2000 | chr12 | 57452022 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57435288
|
C | T | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | NA18956.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.313+89C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435288 | ||||||
| chr12:57435335
|
C | T | 2 | a0003c0003t0008g0372a0003c0003t0008g0373 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.313+136C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435335 | ||||||
| chr12:57435346
|
C | T | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.313+147C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435346 | ||||||
| chr12:57435417
|
T | C | 1 | a0001c0001t0002g0238 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.313+218T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435417 | ||||||
| chr12:57435509
|
A | G | 1 | a0002c0002t0003g0371 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.313+310A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435509 | ||||||
| chr12:57435643
|
G | A | 1 | a0001c0001t0013g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.313+444G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435643 | ||||||
| chr12:57435847
|
CT | C | 6 | a0001c0001t0001g0021a0001c0001t0002g0240a0001c0001t0005g0022others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+662delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57435847 | |||||
| chr12:57435862
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.313+663C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57435862 | ||||||
| chr12:57436134
|
C | T | 95 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(92): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.313+935C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436134 | ||||||
| chr12:57436135
|
G | A | 1 | a0002c0002t0003g0241 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.313+936G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436135 | ||||||
| chr12:57436146
|
C | T | 3 | a0001c0001t0006g0281a0001c0001t0006g0282a0001c0001t0006g0283 | 3 | HG01109.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.313+947C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436146 | ||||||
| chr12:57436161
|
A | T | 2 | a0001c0001t0002g0369a0001c0001t0002g0370 | 2 | NA18997.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.313+962A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436161 | ||||||
| chr12:57436167
|
C | CT | 89 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(86): Show | 95 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+985dupT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57436167 | |||||
| chr12:57436167
|
CT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG01069.hp2 HG01515.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+985delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57436167 | |||||
| chr12:57436289
|
C | T | 9 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(6): Show | 9 | HG02071.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+1090C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436289 | ||||||
| chr12:57436375
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.313+1176C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436375 | ||||||
| chr12:57436384
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+1185C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436384 | ||||||
| chr12:57436473
|
C | CT | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0196others(16): Show | 19 | HG01891.hp2 HG02074.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.313+1293dupT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57436473 | |||||
| chr12:57436473
|
CT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 114 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.313+1293delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57436473 | |||||
| chr12:57436479
|
T | C | 1 | a0001c0001t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.313+1280T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436479 | ||||||
| chr12:57436480
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.313+1281T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436480 | ||||||
| chr12:57436590
|
C | T | 1 | a0002c0002t0003g0280 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.313+1391C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436590 | ||||||
| chr12:57436603
|
C | T | 2 | a0003c0003t0008g0372a0003c0003t0008g0373 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.313+1404C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436603 | ||||||
| chr12:57436811
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.313+1612C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436811 | ||||||
| chr12:57436826
|
C | A | 1 | a0004c0005t0010g0228 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.313+1627C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436826 | ||||||
| chr12:57436933
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.313+1734C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57436933 | ||||||
| chr12:57437040
|
A | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0160others(29): Show | 33 | HG00408.hp2 HG00558.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.313+1841A>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437040 | ||||||
| chr12:57437043
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0091others(35): Show | 40 | HG00558.hp1 HG00609.hp2 HG02027.hp2 others(37): Show |
intron_variant | MODIFIER | c.313+1844C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437043 | ||||||
| chr12:57437166
|
T | C | 5 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+1967T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437166 | ||||||
| chr12:57437262
|
TAAAG | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0193a0002c0002t0003g0279 | 3 | HG02083.hp2 HG02155.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.313+2069_313+2072d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437262 | |||||
| chr12:57437299
|
T | G | 1 | a0001c0001t0002g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.313+2100T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437299 | ||||||
| chr12:57437395
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.313+2196C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437395 | ||||||
| chr12:57437398
|
G | T | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.313+2199G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437398 | ||||||
| chr12:57437497
|
G | A | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.313+2298G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437497 | ||||||
| chr12:57437670
|
C | CA | 138 | a0001c0001t0001g0160a0001c0001t0002g0001a0001c0001t0002g0017others(135): Show | 148 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.313+2486dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437670 | |||||
| chr12:57437670
|
CA | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0159others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+2486delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437670 | |||||
| chr12:57437754
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.313+2555C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437754 | ||||||
| chr12:57437778
|
G | GTGTT | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 87 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.313+2602_313+2605d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437778 | |||||
| chr12:57437778
|
G | GTGTTTGT others(1): Show |
32 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 33 | HG00544.hp1 HG00544.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.313+2598_313+2605d others(10): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437778 | |||||
| chr12:57437778
|
G | GTGTTTGT others(5): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 101 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.313+2594_313+2605d others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437778 | |||||
| chr12:57437778
|
G | GTGTTTGT others(9): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.313+2590_313+2605d others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437778 | |||||
| chr12:57437778
|
GTGTT | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 8 | HG01243.hp2 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+2602_313+2605d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57437778 | |||||
| chr12:57437805
|
A | T | 11 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+2606A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437805 | ||||||
| chr12:57437879
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.313+2680G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437879 | ||||||
| chr12:57437998
|
C | G | 4 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0024others(1): Show | 4 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+2799C>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57437998 | ||||||
| chr12:57438088
|
A | C | 1 | a0001c0001t0002g0357 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.313+2889A>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438088 | ||||||
| chr12:57438201
|
G | A | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.313+3002G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438201 | ||||||
| chr12:57438258
|
TGAATGTT others(10): Show |
T | 1 | a0004c0005t0010g0228 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.313+3061_313+3077d others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57438258 | |||||
| chr12:57438289
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG01109.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.313+3090G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438289 | ||||||
| chr12:57438457
|
T | C | 2 | a0003c0003t0008g0372a0003c0003t0008g0373 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.313+3258T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438457 | ||||||
| chr12:57438489
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01168.hp1 HG02683.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.313+3290A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438489 | ||||||
| chr12:57438655
|
T | A | 370 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(367): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.313+3456T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438655 | ||||||
| chr12:57438708
|
A | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0066others(6): Show | 9 | NA18966.hp2 NA18968.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.313+3509A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438708 | ||||||
| chr12:57439027
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.313+3828C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57439027 | ||||||
| chr12:57439388
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.313+4189A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57439388 | ||||||
| chr12:57439482
|
T | A | 1 | a0002c0002t0003g0245 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.313+4283T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57439482 | ||||||
| chr12:57439607
|
C | A | 1 | a0001c0001t0002g0292 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.313+4408C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57439607 | ||||||
| chr12:57439827
|
G | A | 1 | a0001c0001t0004g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.313+4628G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57439827 | ||||||
| chr12:57440332
|
C | CT | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 110 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+5152dupT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57440332 | |||||
| chr12:57440332
|
C | CTT | 92 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(89): Show | 95 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+5151_313+5152d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57440332 | |||||
| chr12:57440332
|
C | CTTT | 11 | a0001c0001t0002g0001a0001c0001t0002g0285a0001c0001t0002g0290others(8): Show | 13 | HG01106.hp2 HG01109.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+5150_313+5152d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57440332 | |||||
| chr12:57440332
|
CTT | C | 20 | a0001c0001t0001g0141a0001c0001t0002g0011a0001c0001t0002g0142others(17): Show | 21 | HG01167.hp1 HG01169.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.313+5151_313+5152d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57440332 | |||||
| chr12:57440356
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.313+5157C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57440356 | ||||||
| chr12:57440491
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01109.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.313+5292C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57440491 | ||||||
| chr12:57440644
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 189 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.313+5445T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57440644 | ||||||
| chr12:57440960
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0085 | 3 | HG03017.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.313+5761C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57440960 | ||||||
| chr12:57441091
|
C | T | 2 | a0003c0003t0008g0372a0003c0003t0008g0373 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.313+5892C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441091 | ||||||
| chr12:57441128
|
T | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(93): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.313+5929T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441128 | ||||||
| chr12:57441245
|
C | T | 142 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(139): Show | 152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.313+6046C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441245 | ||||||
| chr12:57441302
|
C | T | 16 | a0001c0001t0002g0012a0001c0001t0002g0222a0001c0001t0002g0223others(13): Show | 17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.313+6103C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441302 | ||||||
| chr12:57441309
|
G | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+6110G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441309 | ||||||
| chr12:57441354
|
C | CA | 68 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0028others(65): Show | 69 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.313+6179dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441354 | |||||
| chr12:57441354
|
C | CAA | 13 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0148others(10): Show | 13 | HG00741.hp2 HG02027.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.313+6178_313+6179d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441354 | |||||
| chr12:57441354
|
CA | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0152others(94): Show | 105 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.313+6179delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441354 | |||||
| chr12:57441354
|
CAA | C | 40 | a0001c0001t0002g0350a0002c0002t0003g0013a0002c0002t0003g0014others(37): Show | 44 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.313+6178_313+6179d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441354 | |||||
| chr12:57441382
|
A | G | 370 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(367): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.313+6183A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441382 | ||||||
| chr12:57441402
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(93): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.313+6203G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441402 | ||||||
| chr12:57441520
|
C | T | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.313+6321C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441520 | ||||||
| chr12:57441525
|
C | CA | 15 | a0001c0001t0001g0034a0001c0001t0001g0066a0001c0001t0001g0076others(12): Show | 15 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.313+6345dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441525 | |||||
| chr12:57441525
|
CA | C | 25 | a0001c0001t0001g0060a0001c0001t0001g0140a0001c0001t0001g0143others(22): Show | 26 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.313+6345delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441525 | |||||
| chr12:57441579
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.313+6380A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441579 | ||||||
| chr12:57441685
|
CT | C | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(356): Show | 378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.313+6501delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441685 | |||||
| chr12:57441685
|
CTT | C | 6 | a0001c0001t0002g0303a0001c0001t0004g0124a0001c0001t0004g0125others(3): Show | 6 | HG01256.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.313+6500_313+6501d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57441685 | |||||
| chr12:57441809
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.313+6610G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441809 | ||||||
| chr12:57442006
|
G | C | 5 | a0001c0001t0002g0291a0001c0001t0002g0304a0001c0001t0002g0305others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+6807G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442006 | ||||||
| chr12:57442182
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(93): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.313+6983C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442182 | ||||||
| chr12:57442313
|
T | C | 370 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(367): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.314-6964T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442313 | ||||||
| chr12:57442315
|
A | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(93): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.314-6962A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442315 | ||||||
| chr12:57442646
|
C | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.314-6631C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442646 | ||||||
| chr12:57442747
|
T | A | 2 | a0001c0001t0006g0281a0001c0001t0006g0282 | 2 | HG01109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.314-6530T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442747 | ||||||
| chr12:57442829
|
A | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.314-6448A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442829 | ||||||
| chr12:57442882
|
T | G | 2 | a0001c0001t0002g0306a0001c0001t0002g0358 | 2 | NA18986.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.314-6395T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442882 | ||||||
| chr12:57442914
|
C | A | 1 | a0002c0002t0003g0371 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.314-6363C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442914 | ||||||
| chr12:57442958
|
T | G | 1 | a0001c0001t0002g0359 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.314-6319T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442958 | ||||||
| chr12:57442991
|
C | CA | 37 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0077others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.314-6270dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57442991 | |||||
| chr12:57443066
|
T | C | 2 | a0001c0001t0002g0303a0001c0001t0002g0307 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.314-6211T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443066 | ||||||
| chr12:57443113
|
C | CT | 157 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0056others(154): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.314-6141dupT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57443113 | |||||
| chr12:57443113
|
C | CTT | 71 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0134others(68): Show | 72 | HG00558.hp2 HG00741.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.314-6142_314-6141d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57443113 | |||||
| chr12:57443113
|
C | CTTT | 9 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0166others(6): Show | 9 | HG00408.hp2 HG02818.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-6143_314-6141d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57443113 | |||||
| chr12:57443113
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0057 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.314-6150_314-6141d others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57443113 | |||||
| chr12:57443142
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.314-6135G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443142 | ||||||
| chr12:57443284
|
A | T | 1 | a0001c0001t0004g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.314-5993A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443284 | ||||||
| chr12:57443442
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.314-5835G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443442 | ||||||
| chr12:57443551
|
TGGGATTA others(12): Show |
T | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-5725_314-5707d others(21): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443551 | ||||||
| chr12:57443604
|
A | T | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.314-5673A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443604 | ||||||
| chr12:57443623
|
G | T | 1 | a0002c0002t0003g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.314-5654G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443623 | ||||||
| chr12:57443682
|
A | G | 1 | a0001c0001t0002g0360 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.314-5595A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443682 | ||||||
| chr12:57443789
|
G | A | 4 | a0001c0001t0004g0029a0001c0001t0004g0189a0001c0001t0004g0190others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-5488G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443789 | ||||||
| chr12:57443871
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.314-5406C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57443871 | ||||||
| chr12:57444136
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.314-5141C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444136 | ||||||
| chr12:57444168
|
A | G | 1 | a0001c0001t0002g0336 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314-5109A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444168 | ||||||
| chr12:57444230
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0032 | 2 | HG01256.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.314-5047G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444230 | ||||||
| chr12:57444285
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.314-4992G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444285 | ||||||
| chr12:57444367
|
T | C | 159 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0017others(156): Show | 170 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.314-4910T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444367 | ||||||
| chr12:57444370
|
G | A | 4 | a0001c0001t0004g0029a0001c0001t0004g0189a0001c0001t0004g0190others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-4907G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444370 | ||||||
| chr12:57444542
|
G | GA | 9 | a0001c0001t0001g0039a0001c0001t0001g0159a0001c0001t0002g0204others(6): Show | 9 | HG02055.hp1 HG02080.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.314-4720dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57444542 | |||||
| chr12:57444542
|
GA | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0032others(38): Show | 42 | HG00408.hp2 HG00558.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.314-4720delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57444542 | |||||
| chr12:57444683
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.314-4594A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444683 | ||||||
| chr12:57444724
|
G | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0154others(2): Show | 5 | HG01109.hp2 HG01175.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-4553G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444724 | ||||||
| chr12:57444802
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.314-4475A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57444802 | ||||||
| chr12:57445348
|
G | C | 1 | a0002c0002t0003g0245 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.314-3929G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445348 | ||||||
| chr12:57445377
|
TAAAG | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(3): Show | 6 | HG02280.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-3896_314-3893d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445377 | |||||
| chr12:57445390
|
G | T | 43 | a0002c0002t0003g0013a0002c0002t0003g0014a0002c0002t0003g0015others(40): Show | 47 | HG00639.hp1 HG00738.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.314-3887G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445390 | ||||||
| chr12:57445408
|
TGAG | T | 4 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0024others(1): Show | 4 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-3868_314-3866d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445408 | ||||||
| chr12:57445582
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.314-3695T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445582 | ||||||
| chr12:57445709
|
T | A | 1 | a0001c0001t0002g0285 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.314-3568T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445709 | ||||||
| chr12:57445713
|
A | AC | 109 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0034others(106): Show | 116 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.314-3558dupC | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445713 | |||||
| chr12:57445713
|
A | ACC | 37 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0165others(34): Show | 37 | HG00408.hp1 HG00544.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.314-3559_314-3558d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445713 | |||||
| chr12:57445713
|
A | ACCC | 18 | a0001c0001t0001g0166a0001c0001t0002g0020a0001c0001t0002g0203others(15): Show | 19 | HG00423.hp2 HG01358.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.314-3560_314-3558d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445713 | |||||
| chr12:57445717
|
C | CCG | 12 | a0001c0001t0002g0012a0001c0001t0002g0226a0001c0001t0002g0227others(9): Show | 13 | HG00544.hp1 HG02015.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-3559_314-3558i others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445717 | |||||
| chr12:57445717
|
C | G | 1 | a0002c0002t0003g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.314-3560C>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445717 | ||||||
| chr12:57445718
|
C | A | 3 | a0001c0001t0006g0281a0001c0001t0006g0282a0001c0001t0006g0283 | 3 | HG01109.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.314-3559C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445718 | ||||||
| chr12:57445720
|
G | C | 367 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(364): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.314-3557G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445720 | ||||||
| chr12:57445720
|
G | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0237 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.314-3557G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445720 | ||||||
| chr12:57445721
|
C | G | 1 | a0002c0002t0003g0276 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.314-3556C>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445721 | ||||||
| chr12:57445736
|
A | AT | 132 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0038others(129): Show | 139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.314-3520dupT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445736 | |||||
| chr12:57445736
|
A | ATT | 10 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 10 | HG00738.hp2 HG01981.hp1 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.314-3521_314-3520d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445736 | |||||
| chr12:57445736
|
AT | A | 7 | a0001c0001t0001g0118a0001c0001t0002g0194a0001c0001t0002g0195others(4): Show | 7 | HG01070.hp2 HG02257.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-3520delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57445736 | |||||
| chr12:57445771
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.314-3506C>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445771 | ||||||
| chr12:57445837
|
G | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.314-3440G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57445837 | ||||||
| chr12:57446070
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0159a0001c0001t0015g0087 | 3 | NA18972.hp2 NA19001.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.314-3207G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446070 | ||||||
| chr12:57446242
|
T | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0134others(40): Show | 44 | HG00408.hp2 HG00558.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.314-3035T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446242 | ||||||
| chr12:57446243
|
T | A | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-3034T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446243 | ||||||
| chr12:57446456
|
C | CTTTA | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0160others(9): Show | 13 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-2769_314-2766d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446456
|
CTTTA | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 115 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.314-2769_314-2766d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446456
|
CTTTATTT others(1): Show |
C | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0021others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.314-2773_314-2766d others(10): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446456
|
CTTTATTT others(5): Show |
C | 11 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0065others(8): Show | 12 | HG00621.hp1 HG01243.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-2777_314-2766d others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446456
|
CTTTATTT others(9): Show |
C | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-2781_314-2766d others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446456
|
CTTTATTT others(13): Show |
C | 1 | a0001c0001t0002g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.314-2785_314-2766d others(22): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57446456 | |||||
| chr12:57446525
|
A | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.314-2752A>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446525 | ||||||
| chr12:57446587
|
A | G | 1 | a0001c0001t0004g0124 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.314-2690A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446587 | ||||||
| chr12:57446614
|
C | T | 1 | a0001c0001t0002g0335 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314-2663C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446614 | ||||||
| chr12:57446699
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0142a0001c0001t0002g0197others(17): Show | 21 | HG01167.hp1 HG01169.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.314-2578G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57446699 | ||||||
| chr12:57447139
|
TGGTGAGA others(9): Show |
T | 2 | a0001c0001t0001g0054a0001c0001t0001g0158 | 2 | HG01175.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.314-2135_314-2120d others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447139 | |||||
| chr12:57447266
|
C | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0134others(40): Show | 44 | HG00408.hp2 HG00558.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.314-2011C>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447266 | ||||||
| chr12:57447341
|
C | T | 1 | a0001c0001t0002g0346 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.314-1936C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447341 | ||||||
| chr12:57447350
|
G | A | 143 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(140): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.314-1927G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447350 | ||||||
| chr12:57447553
|
G | A | 1 | a0002c0002t0003g0245 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.314-1724G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447553 | ||||||
| chr12:57447597
|
T | G | 2 | a0003c0003t0008g0372a0003c0003t0008g0373 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.314-1680T>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447597 | ||||||
| chr12:57447797
|
G | A | 16 | a0001c0001t0002g0012a0001c0001t0002g0222a0001c0001t0002g0223others(13): Show | 17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.314-1480G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447797 | ||||||
| chr12:57447862
|
C | CAA | 6 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0174others(3): Show | 6 | HG01168.hp2 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-1385_314-1384d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
C | CAAA | 6 | a0001c0001t0001g0047a0001c0001t0001g0058a0001c0001t0001g0098others(3): Show | 6 | HG00423.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-1386_314-1384d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
C | CAAAA | 6 | a0001c0001t0001g0092a0001c0001t0001g0110a0001c0001t0001g0173others(3): Show | 6 | HG00558.hp2 HG00609.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1387_314-1384d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
CA | C | 8 | a0001c0001t0001g0181a0001c0001t0002g0285a0001c0001t0002g0291others(5): Show | 8 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.314-1384delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
CAA | C | 5 | a0001c0001t0001g0055a0001c0001t0002g0217a0002c0002t0003g0016others(2): Show | 6 | HG01099.hp1 HG01258.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1385_314-1384d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
CAAAAA | C | 6 | a0001c0001t0002g0203a0001c0001t0002g0205a0001c0001t0004g0029others(3): Show | 6 | HG02080.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1388_314-1384d others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447862
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0121others(3): Show | 8 | HG00609.hp1 HG00621.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-1391_314-1384d others(10): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447862 | |||||
| chr12:57447878
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0005g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314-1397_314-1380d others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447878 | |||||
| chr12:57447879
|
AAAAAAAA others(14): Show |
A | 1 | a0002c0002t0003g0267 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.314-1396_314-1376d others(23): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447879 | |||||
| chr12:57447884
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0346 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.314-1393_314-1392i others(15): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447884 | ||||||
| chr12:57447884
|
A | T | 2 | a0001c0001t0001g0053a0001c0001t0002g0305 | 2 | HG01074.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.314-1393A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447884 | ||||||
| chr12:57447886
|
A | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0002g0305others(1): Show | 4 | HG01074.hp2 HG01258.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1391A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447886 | ||||||
| chr12:57447887
|
AAAAAAAT | A | 7 | a0001c0001t0002g0227a0001c0001t0002g0229a0001c0001t0002g0230others(4): Show | 7 | HG02071.hp1 HG02523.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-1388_314-1382d others(9): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447887 | |||||
| chr12:57447887
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0002g0321 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.314-1388_314-1374d others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447887 | |||||
| chr12:57447888
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.314-1388_314-1387i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447888 | |||||
| chr12:57447888
|
A | AATATATA others(7): Show |
2 | a0001c0001t0002g0244a0001c0001t0002g0302 | 2 | HG03225.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.314-1388_314-1387i others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447888 | |||||
| chr12:57447888
|
A | T | 9 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0002g0001others(6): Show | 11 | HG01074.hp2 HG01258.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.314-1389A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447888 | ||||||
| chr12:57447890
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0070 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.314-1386_314-1385i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447890 | |||||
| chr12:57447890
|
A | AATATATA others(7): Show |
1 | a0001c0001t0002g0320 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.314-1386_314-1385i others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447890 | |||||
| chr12:57447890
|
A | AATATATA others(11): Show |
1 | a0001c0001t0002g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.314-1386_314-1385i others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447890 | |||||
| chr12:57447890
|
A | AATATATA others(13): Show |
1 | a0001c0001t0002g0019 | 2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.314-1386_314-1385i others(22): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447890 | |||||
| chr12:57447890
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0356 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.314-1387_314-1386i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447890 | ||||||
| chr12:57447890
|
A | T | 24 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0055others(21): Show | 26 | HG01074.hp2 HG01258.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.314-1387A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447890 | ||||||
| chr12:57447892
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0086 | 2 | HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0078 | 2 | HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0335 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0130 | 2 | HG01243.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0002g0339 | 3 | HG01168.hp1 NA19030.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0309 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0290 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAT others(4): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0064a0001c0001t0015g0087 | 3 | HG01261.hp2 HG04204.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAT others(8): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0054 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0002g0310 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0002g0311 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(23): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAAT others(16): Show |
1 | a0001c0001t0002g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(25): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAAT | 6 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0001g0119others(3): Show | 6 | HG02280.hp1 HG03139.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(8): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(1): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0219others(2): Show | 6 | HG01123.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(10): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(3): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0031others(1): Show | 4 | HG01069.hp2 HG02523.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0089 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(7): Show |
2 | a0001c0001t0001g0002a0001c0001t0002g0312 | 3 | HG03490.hp1 HG03490.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0002g0340 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0011g0289 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0002g0295 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(22): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAATA others(17): Show |
1 | a0001c0001t0002g0313 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(26): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAAT | 6 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0108others(3): Show | 6 | HG01261.hp1 HG02027.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAATAT others(4): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0080a0001c0001t0001g0199others(1): Show | 4 | HG01255.hp2 HG02258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAATAT others(6): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0198a0001c0001t0002g0355 | 3 | HG01175.hp1 HG01175.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(15): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAATAT others(8): Show |
2 | a0001c0001t0001g0021a0001c0001t0002g0369 | 2 | NA19010.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAATAT others(10): Show |
2 | a0001c0001t0002g0322a0001c0001t0002g0370 | 2 | NA18943.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAATAT others(12): Show |
3 | a0001c0001t0002g0303a0001c0001t0002g0307a0001c0001t0002g0329 | 3 | HG01256.hp2 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(21): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAAT | 7 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0107others(4): Show | 7 | HG02040.hp1 HG02165.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATAT | 6 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0094others(3): Show | 6 | HG00738.hp2 HG01346.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(8): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(3): Show |
8 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0067others(5): Show | 8 | HG00099.hp1 HG01069.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(5): Show |
4 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0076others(1): Show | 4 | HG03688.hp1 HG03710.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0157a0001c0001t0002g0331 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(9): Show |
8 | a0001c0001t0001g0050a0001c0001t0001g0090a0001c0001t0002g0301others(5): Show | 8 | HG01358.hp2 HG01978.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0002g0323a0001c0001t0002g0324 | 2 | NA18966.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAAATATA others(13): Show |
3 | a0001c0001t0002g0293a0001c0001t0002g0298a0001c0001t0002g0315 | 3 | HG00741.hp1 NA18951.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(22): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATAT | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0099others(3): Show | 8 | HG00558.hp1 HG02809.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(4): Show |
7 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0075others(4): Show | 7 | HG01071.hp1 HG01517.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(13): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(6): Show |
6 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0071others(3): Show | 6 | HG02683.hp1 HG03669.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(15): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(8): Show |
2 | a0001c0001t0002g0286a0001c0001t0002g0325 | 2 | NA18945.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.314-1384_314-1383i others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(10): Show |
5 | a0001c0001t0002g0306a0001c0001t0002g0316a0001c0001t0002g0334others(2): Show | 5 | NA18947.hp2 NA18968.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-1384_314-1383i others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(12): Show |
1 | a0001c0001t0002g0344 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314-1384_314-1383i others(21): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0002g0330 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(23): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AAATATAT others(16): Show |
1 | a0001c0001t0002g0342 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.314-1384_314-1383i others(25): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATAATAT others(8): Show |
1 | a0001c0001t0002g0363 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.314-1382_314-1381i others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATAT | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0109others(3): Show | 6 | HG02273.hp1 HG03041.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-1357_314-1354d others(6): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0083a0001c0001t0002g0347 | 3 | HG02148.hp2 HG02735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.314-1363_314-1354d others(12): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(5): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0358a0001c0001t0014g0365 | 4 | NA18955.hp1 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-1365_314-1354d others(14): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(7): Show |
1 | a0001c0001t0002g0353 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.314-1367_314-1354d others(16): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(9): Show |
2 | a0001c0001t0002g0341a0001c0001t0002g0354 | 2 | NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.314-1369_314-1354d others(18): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(11): Show |
3 | a0001c0001t0002g0314a0001c0001t0002g0368a0005c0004t0002g0319 | 3 | NA19067.hp2 NA19082.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.314-1371_314-1354d others(20): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AATATATA others(17): Show |
1 | a0001c0001t0002g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.314-1377_314-1354d others(26): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447892 | |||||
| chr12:57447892
|
A | AT | 3 | a0001c0001t0001g0163a0001c0001t0001g0177a0001c0001t0002g0211 | 3 | HG00408.hp2 HG02027.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.314-1385_314-1384i others(3): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447892
|
A | ATATAT | 3 | a0001c0001t0001g0093a0001c0001t0001g0156a0001c0001t0007g0147 | 3 | HG02572.hp1 HG04184.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.314-1385_314-1384i others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447892
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0361 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.314-1385_314-1384i others(17): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447892
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0002g0018a0001c0001t0002g0240a0001c0001t0002g0336 | 4 | HG02083.hp1 NA18962.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1385_314-1384i others(19): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447892
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0327 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.314-1385_314-1384i others(23): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447892
|
A | T | 46 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(43): Show | 49 | HG01074.hp1 HG01074.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.314-1385A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447892 | ||||||
| chr12:57447893
|
AT | A | 11 | a0002c0002t0003g0243a0002c0002t0003g0245a0002c0002t0003g0248others(8): Show | 11 | HG00408.hp1 HG00738.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.314-1383delT | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447893 | ||||||
| chr12:57447893
|
ATAT | A | 11 | a0001c0001t0002g0136a0001c0001t0002g0237a0001c0001t0005g0022others(8): Show | 12 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-1383_314-1381d others(5): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447893 | ||||||
| chr12:57447893
|
ATATAT | A | 4 | a0001c0001t0001g0048a0002c0002t0003g0013a0002c0002t0003g0273others(1): Show | 5 | HG02717.hp2 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-1383_314-1379d others(7): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447893 | ||||||
| chr12:57447893
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-1383_314-1371d others(15): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447893 | ||||||
| chr12:57447894
|
T | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0058a0001c0001t0001g0097others(13): Show | 17 | HG00423.hp1 HG00609.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.314-1383T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447894 | ||||||
| chr12:57447896
|
T | A | 9 | a0001c0001t0001g0047a0002c0002t0003g0242a0002c0002t0003g0250others(6): Show | 9 | HG01106.hp1 HG01167.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-1381T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447896 | ||||||
| chr12:57447898
|
T | A | 7 | a0001c0001t0002g0237a0001c0001t0005g0022a0002c0002t0003g0250others(4): Show | 7 | HG01081.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-1379T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447898 | ||||||
| chr12:57447900
|
T | A | 5 | a0001c0001t0001g0048a0001c0001t0002g0237a0002c0002t0003g0013others(2): Show | 6 | HG02615.hp1 HG02717.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-1377T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447900 | ||||||
| chr12:57447902
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.314-1375T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447902 | ||||||
| chr12:57447906
|
T | A | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-1371T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447906 | ||||||
| chr12:57447907
|
A | C | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-1370A>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447907 | ||||||
| chr12:57447908
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-1369T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447908 | ||||||
| chr12:57447922
|
T | A | 20 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0169others(17): Show | 22 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.314-1355T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447922 | ||||||
| chr12:57447922
|
T | TATATATA others(13): Show |
1 | a0001c0001t0002g0287 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.314-1354_314-1353i others(22): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447922 | |||||
| chr12:57447922
|
TAA | T | 7 | a0002c0002t0003g0242a0002c0002t0003g0251a0002c0002t0003g0256others(4): Show | 7 | HG01361.hp1 HG01975.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-1352_314-1351d others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57447922 | |||||
| chr12:57447924
|
A | T | 34 | a0002c0002t0003g0013a0002c0002t0003g0014a0002c0002t0003g0015others(31): Show | 38 | HG00408.hp1 HG00639.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.314-1353A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447924 | ||||||
| chr12:57447925
|
A | T | 1 | a0001c0001t0002g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314-1352A>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447925 | ||||||
| chr12:57447927
|
T | A | 1 | a0001c0001t0002g0292 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.314-1350T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57447927 | ||||||
| chr12:57448068
|
T | C | 4 | a0001c0001t0004g0029a0001c0001t0004g0189a0001c0001t0004g0190others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1209T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448068 | ||||||
| chr12:57448080
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 179 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.314-1197G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448080 | ||||||
| chr12:57448182
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18961.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.314-1095C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448182 | ||||||
| chr12:57448213
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.314-1064T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448213 | ||||||
| chr12:57448216
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314-1061G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448216 | ||||||
| chr12:57448346
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314-931G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448346 | ||||||
| chr12:57448443
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.314-834C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448443 | ||||||
| chr12:57448505
|
G | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0121others(5): Show | 10 | HG00609.hp1 HG00621.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.314-772G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448505 | ||||||
| chr12:57448526
|
G | A | 1 | a0001c0001t0002g0316 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.314-751G>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448526 | ||||||
| chr12:57448567
|
T | TA | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0121others(10): Show | 15 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-687dupA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57448567 | |||||
| chr12:57448567
|
TA | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 154 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.314-687delA | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57448567 | |||||
| chr12:57448567
|
TAA | T | 18 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0078others(15): Show | 18 | HG00558.hp2 HG01070.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.314-688_314-687del others(2): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57448567 | |||||
| chr12:57448567
|
TAAA | T | 131 | a0001c0001t0001g0104a0001c0001t0002g0001a0001c0001t0002g0017others(128): Show | 141 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.314-689_314-687del others(3): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57448567 | |||||
| chr12:57448567
|
TAAAA | T | 7 | a0001c0001t0002g0308a0001c0001t0002g0330a0001c0001t0002g0350others(4): Show | 7 | HG01109.hp1 HG01346.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-690_314-687del others(4): Show |
INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 57448567 | |||||
| chr12:57448640
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.314-637A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448640 | ||||||
| chr12:57448893
|
T | C | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-384T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448893 | ||||||
| chr12:57448894
|
G | T | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-383G>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448894 | ||||||
| chr12:57448896
|
C | G | 1 | a0002c0002t0003g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.314-381C>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57448896 | ||||||
| chr12:57449006
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.314-271A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57449006 | ||||||
| chr12:57449063
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-214G>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57449063 | ||||||
| chr12:57449172
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.314-105A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57449172 | ||||||
| chr12:57449231
|
C | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.314-46C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57449231 |