Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MTSSL others(347): Show |
chr12 | 57429784 | 57457062 |
| a0002 | 0/0 | 352 | 48 | 10 | 19 | 12 | 2 | 5 | 9 | INHBC_chr12_57429784_57457062 | INHBC | MTSSL others(347): Show |
chr12 | 57429784 | 57457062 |
| a0003 | 0/0 | 352 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | MTSSL others(347): Show |
chr12 | 57429784 | 57457062 |
| a0004 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | MTSSL others(347): Show |
chr12 | 57429784 | 57457062 |
| a0005 | 0/0 | 352 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | MTSSL others(347): Show |
chr12 | 57429784 | 57457062 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1056 | 344 | 75 | 49 | 169 | 10 | 39 | INHBC_chr12_57429784_57457062 | INHBC | ATGAC others(1051): Show |
chr12 | 57429784 | 57457062 | ||
| a0002c0002 | 0/0 | 1056 | 48 | 10 | 19 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | ATGAC others(1051): Show |
chr12 | 57429784 | 57457062 | ||
| a0003c0003 | 0/0 | 1056 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ATGAC others(1051): Show |
chr12 | 57429784 | 57457062 | ||
| a0004c0005 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ATGAC others(1051): Show |
chr12 | 57429784 | 57457062 | ||
| a0005c0004 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ATGAC others(1051): Show |
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 | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0002 | 1/0 | 3202 | 144 | 37 | 17 | 71 | 4 | 14 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0004 | 0/0 | 3202 | 9 | 9 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0005 | 0/0 | 3202 | 4 | 4 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0006 | 0/0 | 3202 | 3 | 2 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0007 | 0/0 | 3202 | 3 | 3 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0011 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0012 | 0/0 | 3202 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0013 | 0/0 | 3202 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0014 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0015 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0016 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0017 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0001c0001t0018 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0002c0002t0003 | 0/0 | 3202 | 47 | 10 | 18 | 12 | 2 | 5 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0002c0002t0009 | 0/0 | 3202 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0003c0003t0008 | 0/0 | 3189 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3184): Show |
chr12 | 57429784 | 57457062 |
| a0004c0005t0010 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| a0005c0004t0002 | 0/0 | 3202 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | ACACT others(3197): Show |
chr12 | 57429784 | 57457062 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0004 | 0/0 | 6 | 1 | 1 | 3 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0005 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0014 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0193 | 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 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0013g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0014g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0016g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0017g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0001c0001t0018g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0001 | 0/0 | 11 | 3 | 4 | 2 | 1 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0002c0002t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0003c0003t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0003c0003t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0004c0005t0010g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| a0005c0004t0002g0015 | 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 | g0003 | EUR | GBR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0268 | EUR | FIN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0217 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0233 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0226 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01081 | hp2 | a0002 | c0002 | t0009 | g0227 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0218 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0245 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0213 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0234 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0229 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0031 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0241 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0247 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0001 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0028 | EUR | IBS | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0310 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0228 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0230 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0240 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02004 | hp1 | a0002 | c0002 | t0003 | g0030 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02071 | hp1 | a0001 | c0001 | t0018 | g0209 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02080 | hp1 | a0001 | c0001 | t0016 | g0197 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0239 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0030 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0235 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0242 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02965 | hp1 | a0003 | c0003 | t0008 | g0312 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0224 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0220 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0238 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0221 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0001 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0222 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0243 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | STU | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CHB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0236 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18957 | hp1 | a0001 | c0001 | t0017 | g0017 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0231 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18972 | hp2 | a0001 | c0001 | t0015 | g0079 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18974 | hp1 | a0004 | c0005 | t0010 | g0204 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18987 | hp1 | a0001 | c0001 | t0011 | g0253 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19056 | hp1 | a0001 | c0001 | t0014 | g0305 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0223 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0207 | 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 | g0083 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | ASW | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0302 | EUR | TSI | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | GIH | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0219 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG06807 | hp1 | a0003 | c0003 | t0008 | g0311 | AFR | USA | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | USA | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA21309 | hp1 | a0005 | c0004 | t0002 | g0015 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | LWK | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0014 | REF | REF | INHBC_chr12_57429784_57457062 | INHBC | chr12 | 57429784 | 57457062 |
| view | 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 |
| view | 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 |
|---|
| view | 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 | a0002c0002t0003 a0002c0002t0009 |
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 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(2): Show |
178 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(175): 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 |
| view | 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 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
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 | a0003c0003t0008g0311 a0003c0003t0008g0312 |
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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | a0001c0001t0002g0212 | 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 | a0002c0002t0003g0310 | 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 | a0001c0001t0013g0213 | 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 | a0001c0001t0001g0036 a0001c0001t0002g0214 a0001c0001t0005g0037 others(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 | a0001c0001t0002g0211 | 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 | 76 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(73): 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 | a0002c0002t0003g0215 | 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 | a0001c0001t0006g0244 a0001c0001t0006g0245 a0001c0001t0006g0246 |
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 | a0001c0001t0002g0248 a0001c0001t0002g0306 |
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 | 78 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(75): 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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | 8 | a0001c0001t0002g0027 a0001c0001t0002g0205 a0001c0001t0002g0206 others(5): 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0174 others(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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
113 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(110): 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 | a0001c0001t0002g0250 | 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 | a0001c0001t0001g0036 | 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 | a0002c0002t0003g0243 | 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 | a0003c0003t0008g0311 a0003c0003t0008g0312 |
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 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
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 | a0004c0005t0010g0204 | 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 | a0001c0001t0001g0165 | 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 | 31 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(28): 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 | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): 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 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0002c0002t0003g0242 |
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 | a0001c0001t0002g0255 | 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 | a0001c0001t0001g0082 | 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | 109 | a0001c0001t0001g0140 a0001c0001t0002g0002 a0001c0001t0002g0004 others(106): 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 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0107 | 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 | 80 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(77): 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 |
31 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(28): 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 |
72 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
100 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(97): 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | 6 | a0001c0001t0001g0013 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
10 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(7): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(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 | a0001c0001t0002g0297 | 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | a0004c0005t0010g0204 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | a0003c0003t0008g0311 a0003c0003t0008g0312 |
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 | 1 | a0001c0001t0001g0012 | 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 | 310 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.313+3456T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57438655 | |||||||
| chr12:57438708 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0048 others(4): 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0088 | 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 | a0002c0002t0003g0217 | 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 | a0001c0001t0002g0256 | 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 | a0001c0001t0004g0044 | 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 | 91 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(88): 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 | 72 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(69): 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 | a0001c0001t0002g0016 a0001c0001t0002g0249 a0001c0001t0002g0254 others(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 | 19 | a0001c0001t0001g0123 a0001c0001t0002g0024 a0001c0001t0002g0025 others(16): 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | 153 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
188 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(185): 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0077 |
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 | a0003c0003t0008g0311 a0003c0003t0008g0312 |
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 | 77 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(74): 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 | 113 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): 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 | 15 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0198 others(12): 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 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | 67 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0042 others(64): 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 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | 78 | a0001c0001t0001g0021 a0001c0001t0001g0085 a0001c0001t0001g0132 others(75): 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 | 30 | a0001c0001t0002g0290 a0002c0002t0003g0001 a0002c0002t0003g0028 others(27): 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 | 310 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.313+6183A>G | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57441382 | |||||||
| chr12:57441402 | G | A | 77 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(74): 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 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0073 others(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 | 24 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0125 others(21): 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 | a0001c0001t0001g0064 | 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 | 299 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): 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 | a0001c0001t0002g0267 a0001c0001t0004g0108 a0001c0001t0004g0109 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0255 a0001c0001t0002g0268 a0001c0001t0002g0269 others(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 | 77 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(74): 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 | 310 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.314-6964T>C | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442313 | |||||||
| chr12:57442315 | A | G | 77 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(74): 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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG01109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.314-6530T>A | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57442747 | |||||||
| chr12:57442882 | T | G | 2 | a0001c0001t0002g0270 a0001c0001t0002g0298 |
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 | a0002c0002t0003g0310 | 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 | a0001c0001t0002g0299 | 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 | 36 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(33): 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 | a0001c0001t0002g0267 a0001c0001t0002g0271 |
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 | 128 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0061 others(125): 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 | 69 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0117 others(66): 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 | 8 | a0001c0001t0001g0023 a0001c0001t0001g0140 a0001c0001t0001g0145 others(5): 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0004g0110 | 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 | a0001c0001t0002g0254 | 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 | a0002c0002t0003g0218 | 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | a0002c0002t0003g0237 | 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 | a0001c0001t0002g0300 | 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 | a0001c0001t0004g0044 a0001c0001t0004g0167 a0001c0001t0004g0168 others(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 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0002g0280 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0158 | 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 | 129 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(126): 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 | a0001c0001t0004g0044 a0001c0001t0004g0167 a0001c0001t0004g0168 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0139 a0001c0001t0002g0182 others(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 | 39 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(36): 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0059 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0104 | 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 | a0002c0002t0003g0217 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | 33 | a0002c0002t0003g0001 a0002c0002t0003g0028 a0002c0002t0003g0029 others(30): 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 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0002g0249 | 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 | 98 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(95): 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 | 35 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0145 others(32): 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 | 14 | a0001c0001t0001g0146 a0001c0001t0002g0005 a0001c0001t0002g0181 others(11): 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 | 11 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0202 others(8): 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 | a0002c0002t0003g0242 | 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 | a0001c0001t0006g0244 a0001c0001t0006g0245 a0001c0001t0006g0246 |
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 | 307 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(304): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): 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 | a0001c0001t0002g0166 a0001c0001t0002g0211 |
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 | a0002c0002t0003g0241 | 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 | 112 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(109): 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 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0102 a0001c0001t0002g0172 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0139 a0001c0001t0015g0079 |
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 | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(38): 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 | a0002c0002t0003g0218 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0140 others(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 | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(87): 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 | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(166): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): 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 | 10 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0068 others(7): 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0002g0272 | 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | a0001c0001t0004g0108 | 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 | a0001c0001t0002g0279 | 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 | 19 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0124 others(16): 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 | a0001c0001t0001g0059 a0001c0001t0001g0138 |
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 | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0043 others(38): 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 | a0001c0001t0002g0286 | 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 | 114 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): 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 | a0002c0002t0003g0217 | 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 | a0003c0003t0008g0311 a0003c0003t0008g0312 |
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 | 15 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0198 others(12): 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 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0100 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0159 a0001c0001t0002g0249 a0001c0001t0002g0255 others(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 | a0001c0001t0001g0060 a0001c0001t0002g0193 a0002c0002t0003g0030 others(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 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0004g0044 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0105 others(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 | a0001c0001t0005g0039 | 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 | a0002c0002t0003g0001 | 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 | a0001c0001t0002g0286 | 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 | a0001c0001t0001g0003 a0001c0001t0002g0269 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0002g0269 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0203 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0274 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0216 a0001c0001t0002g0266 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0002g0002 | 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 | a0001c0001t0002g0296 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0078 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0075 |
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 | a0001c0001t0001g0013 | 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 | a0001c0001t0002g0279 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0113 |
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 |
2 | a0001c0001t0001g0012 a0001c0001t0002g0283 |
2 | HG01168.hp1 NA19030.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(7): Show |
1 | a0001c0001t0002g0004 | 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 | a0001c0001t0002g0254 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0015g0079 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0059 |
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 | a0001c0001t0002g0004 | 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 | a0001c0001t0002g0004 | 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0095 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0002g0034 | 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 | a0001c0001t0011g0253 | 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 | a0001c0001t0002g0259 | 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 | a0001c0001t0002g0004 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0176 a0001c0001t0002g0295 |
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 | a0001c0001t0001g0036 a0001c0001t0002g0248 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0306 |
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 | a0001c0001t0002g0267 a0001c0001t0002g0271 a0001c0001t0002g0277 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0137 a0001c0001t0002g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0275 |
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 | a0001c0001t0002g0033 a0001c0001t0002g0257 a0001c0001t0002g0262 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0069 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0250 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0270 a0001c0001t0002g0273 others(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 | a0001c0001t0002g0035 | 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 | a0001c0001t0002g0278 | 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 | a0001c0001t0002g0284 | 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 | a0001c0001t0002g0303 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0002g0287 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0298 a0001c0001t0014g0305 |
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 | a0001c0001t0002g0293 | 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 | a0001c0001t0002g0034 a0001c0001t0002g0294 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0309 a0005c0004t0002g0015 |
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 | a0001c0001t0002g0002 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0002g0188 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0136 a0001c0001t0007g0019 |
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 | a0001c0001t0002g0301 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0280 |
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 | a0001c0001t0002g0002 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | 10 | a0002c0002t0003g0001 a0002c0002t0003g0028 a0002c0002t0003g0217 others(7): 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 | a0001c0001t0002g0014 a0001c0001t0002g0211 a0001c0001t0005g0037 others(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 | a0001c0001t0001g0057 a0002c0002t0003g0029 a0002c0002t0003g0031 others(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 | a0001c0001t0001g0174 | 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 | 13 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0089 others(10): 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 | 7 | a0001c0001t0001g0056 a0002c0002t0003g0001 a0002c0002t0003g0028 others(4): 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 | a0001c0001t0002g0211 a0001c0001t0005g0037 a0002c0002t0003g0222 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0211 a0002c0002t0003g0029 others(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 | a0001c0001t0001g0086 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0001c0001t0001g0174 | 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 | 19 | a0001c0001t0001g0142 a0001c0001t0001g0148 a0001c0001t0001g0149 others(16): 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 | a0001c0001t0002g0251 | 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 | 6 | a0002c0002t0003g0001 a0002c0002t0003g0028 a0002c0002t0003g0031 others(3): 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 | 29 | a0002c0002t0003g0001 a0002c0002t0003g0028 a0002c0002t0003g0029 others(26): 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 | a0001c0001t0002g0193 | 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 | a0001c0001t0002g0256 | 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 | a0001c0001t0004g0044 a0001c0001t0004g0167 a0001c0001t0004g0168 others(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 | 143 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
178 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(175): 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0171 | 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 | a0001c0001t0002g0166 | 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 | a0001c0001t0002g0188 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0105 others(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 | a0001c0001t0002g0273 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0105 others(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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(150): 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 | 15 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0058 others(12): 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 | 102 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0004 others(99): 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 | a0001c0001t0002g0272 a0001c0001t0002g0278 a0001c0001t0002g0290 others(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 | a0001c0001t0002g0285 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0117 | 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 | 256 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.314-46C>T | INHBC | ENSG00000175189.4 | transcript | ENST00000309668.3 | protein_coding | 1/1 | chr12 | 57449231 |