Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 64423 |
|---|---|
| ensemblid | ENSG00000203485.14 |
| hgncid | 23791 |
| symbol | INF2 |
| name | inverted formin 2 |
| refseq_nuc | NM_022489.4 |
| refseq_prot | NP_071934.3 |
| ensembl_nuc | ENST00000392634.9 |
| ensembl_prot | ENSP00000376410.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 104689618 |
| end | 104722535 |
| strand | + |
| ver | v1.2 |
| region | chr14:104689618-104722535 |
| region5000 | chr14:104684618-104727535 |
| regionname0 | INF2_chr14_104689618_104722535 |
| regionname5000 | INF2_chr14_104684618_104727535 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1249 | 282 | 63 | 63 | 116 | 10 | 28 | 83 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002 | 0/0 | 1245 | 32 | 5 | 6 | 10 | 3 | 8 | 6 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003 | 0/0 | 1247 | 10 | 7 | 1 | 1 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004 | 0/0 | 1247 | 7 | 2 | 2 | 1 | 0 | 2 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0005 | 0/0 | 1249 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0006 | 0/0 | 1249 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0007 | 0/0 | 1247 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0008 | 0/0 | 1249 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0009 | 0/0 | 1249 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0010 | 0/0 | 1249 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0011 | 0/0 | 1249 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0012 | 0/0 | 1249 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0013 | 0/0 | 1249 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0014 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0015 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0016 | 0/0 | 1247 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0017 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0018 | 0/0 | 1249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0019 | 0/0 | 1249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0020 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0021 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0022 | 0/0 | 1249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0023 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0024 | 0/0 | 1249 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0025 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0026 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0027 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3750 | 187 | 39 | 37 | 86 | 7 | 17 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0002 | 0/0 | 3750 | 35 | 11 | 17 | 1 | 3 | 3 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0003 | 0/0 | 3738 | 26 | 0 | 6 | 10 | 2 | 8 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0004 | 0/0 | 3750 | 26 | 0 | 4 | 17 | 0 | 5 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0005 | 0/0 | 3750 | 8 | 7 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0006 | 0/0 | 3744 | 7 | 2 | 2 | 1 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0007 | 0/0 | 3750 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0008 | 0/0 | 3750 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0009 | 0/0 | 3750 | 5 | 0 | 0 | 3 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0010 | 0/0 | 3744 | 5 | 5 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0011 | 0/0 | 3750 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0012 | 0/0 | 3744 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0013 | 0/0 | 3738 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0014 | 0/0 | 3750 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0015 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0016 | 0/0 | 3750 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0017 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0018 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0019 | 0/0 | 3744 | 3 | 0 | 1 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0020 | 0/0 | 3750 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0021 | 0/0 | 3750 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0022 | 0/0 | 3750 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0023 | 0/0 | 3750 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0024 | 0/0 | 3750 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0025 | 0/0 | 3750 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0026 | 1/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0027 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0028 | 0/0 | 3737 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0029 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0030 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0031 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0032 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0033 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0034 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0035 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0036 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0037 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0038 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0039 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0040 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0041 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0042 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0043 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0044 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0045 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0046 | 0/0 | 3738 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0047 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0048 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0049 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0050 | 0/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0051 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| c0052 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3834 | 100 | 17 | 21 | 49 | 4 | 9 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0002 | 0/0 | 3834 | 35 | 1 | 8 | 24 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0003 | 0/0 | 3839 | 27 | 7 | 12 | 1 | 4 | 3 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0004 | 0/0 | 3869 | 13 | 0 | 6 | 7 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0005 | 0/0 | 3832 | 12 | 12 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0006 | 0/0 | 4013 | 10 | 0 | 2 | 4 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0007 | 0/0 | 3835 | 8 | 0 | 0 | 8 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0008 | 0/1 | 3904 | 7 | 2 | 1 | 2 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0009 | 0/0 | 4013 | 6 | 0 | 1 | 0 | 1 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0010 | 0/0 | 3977 | 6 | 0 | 0 | 6 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0011 | 0/0 | 3833 | 5 | 4 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0012 | 0/0 | 3834 | 5 | 4 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0013 | 0/0 | 3834 | 5 | 0 | 3 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0014 | 0/0 | 3869 | 5 | 0 | 1 | 2 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0015 | 0/0 | 3939 | 5 | 0 | 0 | 3 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0016 | 0/0 | 4013 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0017 | 0/0 | 3833 | 4 | 3 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0018 | 0/0 | 3839 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0019 | 0/0 | 3839 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0020 | 0/0 | 3834 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0021 | 0/0 | 3834 | 3 | 0 | 0 | 1 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0022 | 0/0 | 3834 | 3 | 0 | 2 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0023 | 0/0 | 3764 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0024 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0025 | 0/0 | 3944 | 3 | 1 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0026 | 0/0 | 3832 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0027 | 0/0 | 3765 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0028 | 0/0 | 3765 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0029 | 0/0 | 3869 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0030 | 0/0 | 3834 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0031 | 0/0 | 3979 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0032 | 0/0 | 3944 | 2 | 1 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0033 | 0/0 | 3904 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0034 | 0/0 | 3839 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0035 | 0/0 | 3833 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0036 | 0/0 | 3833 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0037 | 0/0 | 3660 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0038 | 0/0 | 3972 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0039 | 0/0 | 3978 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0040 | 0/0 | 4048 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0041 | 0/0 | 3944 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0042 | 0/0 | 3833 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0043 | 0/0 | 3834 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0044 | 0/0 | 3905 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0045 | 0/0 | 4149 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0046 | 0/0 | 3765 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0047 | 0/0 | 3869 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0048 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0049 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0050 | 0/0 | 3841 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0051 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0052 | 0/0 | 4013 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0053 | 0/0 | 3833 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0054 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0055 | 0/0 | 3944 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0056 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0057 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0058 | 0/0 | 3804 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0059 | 0/0 | 3765 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0060 | 0/0 | 3869 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0061 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0062 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0063 | 0/0 | 3943 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0064 | 1/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0065 | 0/0 | 4048 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0066 | 0/0 | 3833 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0067 | 0/0 | 3839 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0068 | 0/0 | 3839 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0069 | 0/0 | 3806 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0070 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0071 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0072 | 0/0 | 3832 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0073 | 0/0 | 3832 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0074 | 0/0 | 3797 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0075 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0076 | 0/0 | 3869 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0077 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0078 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0079 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0080 | 0/0 | 4237 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0081 | 0/0 | 3834 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0082 | 0/0 | 3940 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0083 | 0/0 | 3870 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0084 | 0/0 | 3800 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0085 | 0/0 | 3772 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0086 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0087 | 0/0 | 3834 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0088 | 0/0 | 3487 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0089 | 0/0 | 3834 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0090 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0091 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0092 | 0/0 | 3905 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0093 | 0/0 | 3730 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0094 | 0/0 | 3382 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0095 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0096 | 0/0 | 3798 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| t0097 | 0/0 | 3834 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 22 | 0 | 7 | 14 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0002 | 0/0 | 17 | 1 | 6 | 7 | 0 | 3 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0003 | 0/0 | 13 | 0 | 9 | 0 | 2 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0004 | 0/0 | 10 | 0 | 4 | 5 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0005 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0007 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0026 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3750 | 187 | 39 | 37 | 86 | 7 | 17 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002 | 0/0 | 3750 | 35 | 11 | 17 | 1 | 3 | 3 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004 | 0/0 | 3750 | 26 | 0 | 4 | 17 | 0 | 5 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005 | 0/0 | 3750 | 8 | 7 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0009 | 0/0 | 3750 | 5 | 0 | 0 | 3 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0014 | 0/0 | 3750 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0017 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0020 | 0/0 | 3750 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0021 | 0/0 | 3750 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0022 | 0/0 | 3750 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0025 | 0/0 | 3750 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0026 | 1/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0031 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0035 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0036 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0038 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0041 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0051 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003 | 0/0 | 3738 | 26 | 0 | 6 | 10 | 2 | 8 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0013 | 0/0 | 3738 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0046 | 0/0 | 3738 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0047 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0010 | 0/0 | 3744 | 5 | 5 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0019 | 0/0 | 3744 | 3 | 0 | 1 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0043 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0044 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006 | 0/0 | 3744 | 7 | 2 | 2 | 1 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0005c0008 | 0/0 | 3750 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0006c0007 | 0/0 | 3750 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0007c0012 | 0/0 | 3744 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0008c0016 | 0/0 | 3750 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0008c0029 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0009c0015 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0009c0032 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0010c0011 | 0/0 | 3750 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0011c0018 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0012c0023 | 0/0 | 3750 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0013c0024 | 0/0 | 3750 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0014c0028 | 0/0 | 3737 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0015c0048 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0016c0042 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0017c0045 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0018c0034 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0019c0033 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0020c0030 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0021c0037 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0022c0039 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0023c0040 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0024c0050 | 0/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0025c0049 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0026c0027 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0027c0052 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7583 | 64 | 15 | 14 | 27 | 4 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0002 | 0/0 | 7583 | 27 | 1 | 2 | 22 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0003 | 0/0 | 7588 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0004 | 0/0 | 7618 | 9 | 0 | 5 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0005 | 0/0 | 7581 | 9 | 9 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0007 | 0/0 | 7584 | 8 | 0 | 0 | 8 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0008 | 0/1 | 7653 | 6 | 2 | 1 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0012 | 0/0 | 7583 | 5 | 4 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0013 | 0/0 | 7583 | 5 | 0 | 3 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0014 | 0/0 | 7618 | 4 | 0 | 1 | 1 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0015 | 0/0 | 7688 | 4 | 0 | 0 | 3 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0020 | 0/0 | 7583 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0021 | 0/0 | 7583 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0022 | 0/0 | 7583 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0026 | 0/0 | 7581 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0027 | 0/0 | 7514 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0030 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0033 | 0/0 | 7653 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0036 | 0/0 | 7582 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0038 | 0/0 | 7721 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0040 | 0/0 | 7797 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0043 | 0/0 | 7583 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0044 | 0/0 | 7654 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0057 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0059 | 0/0 | 7514 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0063 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0072 | 0/0 | 7581 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0073 | 0/0 | 7581 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0074 | 0/0 | 7546 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0075 | 0/0 | 7616 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0076 | 0/0 | 7618 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0077 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0081 | 0/0 | 7583 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0082 | 0/0 | 7689 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0083 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0085 | 0/0 | 7521 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0086 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0087 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0088 | 0/0 | 7236 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0089 | 0/0 | 7583 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0090 | 0/0 | 7653 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0091 | 0/0 | 7724 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0092 | 0/0 | 7654 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0093 | 0/0 | 7479 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0094 | 0/0 | 7131 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0095 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0001t0096 | 0/0 | 7547 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0003 | 0/0 | 7588 | 23 | 6 | 10 | 1 | 3 | 3 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0011 | 0/0 | 7582 | 5 | 4 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0019 | 0/0 | 7588 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0034 | 0/0 | 7588 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0058 | 0/0 | 7553 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0002t0066 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004t0001 | 0/0 | 7583 | 22 | 0 | 4 | 14 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004t0014 | 0/0 | 7618 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004t0015 | 0/0 | 7688 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004t0027 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0004t0080 | 0/0 | 7986 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005t0023 | 0/0 | 7513 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005t0035 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005t0036 | 0/0 | 7582 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005t0042 | 0/0 | 7582 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0005t0062 | 0/0 | 7547 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0009t0009 | 0/0 | 7762 | 2 | 0 | 0 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0009t0010 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0009t0040 | 0/0 | 7797 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0009t0065 | 0/0 | 7797 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0014t0029 | 0/0 | 7618 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0017t0005 | 0/0 | 7581 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0020t0047 | 0/0 | 7618 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0020t0060 | 0/0 | 7618 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0021t0001 | 0/0 | 7583 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0021t0097 | 0/0 | 7583 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0022t0069 | 0/0 | 7555 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0022t0070 | 0/0 | 7554 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0025t0002 | 0/0 | 7583 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0026t0064 | 1/0 | 7622 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0031t0004 | 0/0 | 7618 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0035t0079 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0036t0008 | 0/0 | 7653 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0038t0024 | 0/0 | 7616 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0041t0030 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0001c0051t0004 | 0/0 | 7618 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0006 | 0/0 | 7750 | 10 | 0 | 2 | 4 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0009 | 0/0 | 7750 | 3 | 0 | 1 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0010 | 0/0 | 7714 | 5 | 0 | 0 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0031 | 0/0 | 7716 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0039 | 0/0 | 7715 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0048 | 0/0 | 7855 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0049 | 0/0 | 7855 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0052 | 0/0 | 7750 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0003t0071 | 0/0 | 7714 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0013t0016 | 0/0 | 7750 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0046t0001 | 0/0 | 7571 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0002c0047t0003 | 0/0 | 7576 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0010t0018 | 0/0 | 7582 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0010t0067 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0010t0068 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0019t0021 | 0/0 | 7577 | 2 | 0 | 0 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0019t0022 | 0/0 | 7577 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0043t0025 | 0/0 | 7687 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0003c0044t0053 | 0/0 | 7576 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006t0032 | 0/0 | 7687 | 2 | 1 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006t0041 | 0/0 | 7687 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006t0054 | 0/0 | 7757 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006t0055 | 0/0 | 7687 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0004c0006t0056 | 0/0 | 7687 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0005c0008t0002 | 0/0 | 7583 | 2 | 0 | 1 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0005c0008t0004 | 0/0 | 7618 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0005c0008t0045 | 0/0 | 7898 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0006c0007t0001 | 0/0 | 7583 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0007c0012t0001 | 0/0 | 7577 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0007c0012t0028 | 0/0 | 7508 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0008c0016t0002 | 0/0 | 7583 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0008c0029t0003 | 0/0 | 7588 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0009c0015t0017 | 0/0 | 7582 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0009c0032t0017 | 0/0 | 7582 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0010c0011t0001 | 0/0 | 7583 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0010c0011t0046 | 0/0 | 7514 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0011c0018t0024 | 0/0 | 7616 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0011c0018t0061 | 0/0 | 7616 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0012c0023t0025 | 0/0 | 7693 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0013c0024t0037 | 0/0 | 7409 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0014c0028t0051 | 0/0 | 7749 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0015c0048t0050 | 0/0 | 7578 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0016c0042t0022 | 0/0 | 7577 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0017c0045t0018 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0018c0034t0001 | 0/0 | 7583 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0019c0033t0003 | 0/0 | 7588 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0020c0030t0078 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0021c0037t0002 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0022c0039t0035 | 0/0 | 7582 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0023c0040t0084 | 0/0 | 7549 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0024c0050t0001 | 0/0 | 7583 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0025c0049t0009 | 0/0 | 7750 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0026c0027t0001 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| a0027c0052t0030 | 0/0 | 7583 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | copy fasta | chr14 | 104684618 | 104727535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0007g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0012g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0013g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0014g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0014g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0015g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0020g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0020g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0022g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0026g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0027g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0027g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0030g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0033g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0036g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0038g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0040g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0043g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0043g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0044g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0057g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0059g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0063g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0072g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0073g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0074g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0075g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0076g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0077g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0081g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0082g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0083g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0085g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0086g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0087g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0088g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0089g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0090g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0091g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0092g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0093g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0094g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0095g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0001t0096g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0003 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0011g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0011g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0019g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0034g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0058g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0002t0066g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0004 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0014g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0015g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0027g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0004t0080g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0023g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0023g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0035g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0036g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0042g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0042g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0005t0062g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0009t0009g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0009t0009g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0009t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0009t0040g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0009t0065g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0014t0029g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0014t0029g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0017t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0017t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0020t0047g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0020t0060g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0021t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0021t0097g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0022t0069g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0022t0070g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0025t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0026t0064g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0031t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0035t0079g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0036t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0038t0024g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0041t0030g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0001c0051t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0009g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0010g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0010g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0031g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0031g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0039g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0048g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0049g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0052g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0003t0071g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0013t0016g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0013t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0013t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0046t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0002c0047t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0010t0018g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0010t0018g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0010t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0010t0067g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0010t0068g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0019t0021g0026 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0019t0022g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0043t0025g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0003c0044t0053g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0032g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0032g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0041g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0041g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0054g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0055g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0004c0006t0056g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0005c0008t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0005c0008t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0005c0008t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0005c0008t0045g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0006c0007t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0006c0007t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0006c0007t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0006c0007t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0007c0012t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0007c0012t0028g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0007c0012t0028g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0008c0016t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0008c0016t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0008c0029t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0009c0015t0017g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0009c0032t0017g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0010c0011t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0010c0011t0046g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0010c0011t0046g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0011c0018t0024g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0011c0018t0061g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0012c0023t0025g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0012c0023t0025g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0013c0024t0037g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0014c0028t0051g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0015c0048t0050g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0016c0042t0022g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0017c0045t0018g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0018c0034t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0019c0033t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0020c0030t0078g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0021c0037t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0022c0039t0035g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0023c0040t0084g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0024c0050t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0025c0049t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0026c0027t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| a0027c0052t0030g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0031 | g0007 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0003 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00280 | hp1 | a0001 | c0001 | t0075 | g0148 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00280 | hp2 | a0002 | c0003 | t0039 | g0030 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00323 | hp1 | a0025 | c0049 | t0009 | g0125 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00423 | hp1 | a0001 | c0001 | t0087 | g0203 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00423 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0033 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00544 | hp1 | a0001 | c0004 | t0080 | g0021 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00544 | hp2 | a0006 | c0007 | t0001 | g0002 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00558 | hp2 | a0020 | c0030 | t0078 | g0005 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00597 | hp1 | a0001 | c0001 | t0027 | g0002 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00609 | hp2 | a0005 | c0008 | t0002 | g0212 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00621 | hp1 | a0001 | c0001 | t0090 | g0138 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00639 | hp1 | a0001 | c0002 | t0058 | g0117 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00642 | hp2 | a0008 | c0016 | t0002 | g0198 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00673 | hp2 | a0002 | c0003 | t0010 | g0007 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00733 | hp2 | a0009 | c0032 | t0017 | g0107 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0040 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00735 | hp2 | a0004 | c0006 | t0041 | g0108 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0123 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG00741 | hp2 | a0001 | c0001 | t0059 | g0110 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01069 | hp2 | a0001 | c0002 | t0019 | g0019 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01071 | hp1 | a0001 | c0002 | t0019 | g0019 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01074 | hp1 | a0001 | c0002 | t0011 | g0167 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0077 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01081 | hp2 | a0001 | c0001 | t0036 | g0111 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0094 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01099 | hp2 | a0016 | c0042 | t0022 | g0097 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01106 | hp1 | a0001 | c0021 | t0097 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01106 | hp2 | a0002 | c0003 | t0049 | g0229 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01109 | hp2 | a0002 | c0003 | t0031 | g0234 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01167 | hp1 | a0001 | c0001 | t0038 | g0028 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01168 | hp2 | a0001 | c0025 | t0002 | g0001 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01169 | hp1 | a0001 | c0025 | t0002 | g0001 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01169 | hp2 | a0001 | c0001 | t0038 | g0028 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01175 | hp2 | a0001 | c0002 | t0019 | g0019 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0074 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01192 | hp2 | a0019 | c0033 | t0003 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01243 | hp2 | a0004 | c0006 | t0056 | g0027 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01256 | hp1 | a0001 | c0002 | t0034 | g0003 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01256 | hp2 | a0018 | c0034 | t0001 | g0058 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01257 | hp1 | a0001 | c0001 | t0033 | g0037 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01257 | hp2 | a0002 | c0003 | t0006 | g0052 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01258 | hp1 | a0001 | c0001 | t0033 | g0037 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01258 | hp2 | a0001 | c0002 | t0034 | g0003 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01261 | hp2 | a0001 | c0001 | t0013 | g0120 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01358 | hp1 | a0008 | c0016 | t0002 | g0045 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0197 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01361 | hp2 | a0002 | c0003 | t0009 | g0025 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01433 | hp2 | a0002 | c0003 | t0006 | g0052 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01496 | hp1 | a0001 | c0021 | t0001 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0003 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01516 | hp1 | a0001 | c0001 | t0014 | g0035 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01516 | hp2 | a0013 | c0024 | t0037 | g0029 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0080 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01517 | hp2 | a0001 | c0001 | t0014 | g0035 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01884 | hp1 | a0003 | c0044 | t0053 | g0099 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01884 | hp2 | a0001 | c0001 | t0073 | g0226 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01891 | hp2 | a0001 | c0005 | t0042 | g0175 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01928 | hp1 | a0001 | c0001 | t0088 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01934 | hp1 | a0003 | c0019 | t0022 | g0095 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01943 | hp1 | a0006 | c0007 | t0001 | g0039 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0082 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01975 | hp1 | a0008 | c0016 | t0002 | g0045 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01978 | hp2 | a0005 | c0008 | t0002 | g0195 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01981 | hp1 | a0013 | c0024 | t0037 | g0029 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01981 | hp2 | a0001 | c0001 | t0076 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02015 | hp2 | a0001 | c0004 | t0014 | g0062 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02055 | hp1 | a0007 | c0012 | t0001 | g0127 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02056 | hp2 | a0001 | c0001 | t0015 | g0008 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02071 | hp1 | a0001 | c0001 | t0027 | g0160 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02074 | hp1 | a0003 | c0019 | t0021 | g0026 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02074 | hp2 | a0001 | c0001 | t0086 | g0069 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02083 | hp1 | a0001 | c0001 | t0057 | g0103 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02083 | hp2 | a0002 | c0003 | t0006 | g0232 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02132 | hp2 | a0001 | c0020 | t0047 | g0239 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02135 | hp2 | a0001 | c0001 | t0015 | g0151 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02148 | hp1 | a0001 | c0051 | t0004 | g0201 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0240 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02257 | hp2 | a0001 | c0005 | t0023 | g0164 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02258 | hp1 | a0001 | c0001 | t0074 | g0131 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02280 | hp1 | a0001 | c0038 | t0024 | g0178 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02280 | hp2 | a0009 | c0015 | t0017 | g0014 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02300 | hp2 | a0002 | c0003 | t0052 | g0241 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02451 | hp1 | a0003 | c0043 | t0025 | g0100 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02523 | hp1 | a0002 | c0003 | t0006 | g0233 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02523 | hp2 | a0001 | c0001 | t0095 | g0208 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02572 | hp1 | a0002 | c0013 | t0016 | g0184 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02572 | hp2 | a0003 | c0010 | t0018 | g0054 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0003 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02602 | hp2 | a0001 | c0001 | t0044 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02615 | hp1 | a0001 | c0017 | t0005 | g0181 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0093 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02622 | hp1 | a0002 | c0013 | t0016 | g0042 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02630 | hp2 | a0017 | c0045 | t0018 | g0054 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02647 | hp1 | a0001 | c0017 | t0005 | g0049 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02647 | hp2 | a0011 | c0018 | t0024 | g0041 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02698 | hp2 | a0001 | c0009 | t0009 | g0114 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02717 | hp1 | a0001 | c0001 | t0072 | g0227 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0088 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0024 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0132 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02735 | hp2 | a0001 | c0001 | t0008 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02809 | hp1 | a0011 | c0018 | t0061 | g0165 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02809 | hp2 | a0001 | c0002 | t0011 | g0168 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0092 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02818 | hp2 | a0001 | c0005 | t0023 | g0113 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02886 | hp1 | a0001 | c0022 | t0069 | g0118 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02886 | hp2 | a0001 | c0017 | t0005 | g0049 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02922 | hp2 | a0003 | c0010 | t0067 | g0243 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02965 | hp1 | a0001 | c0022 | t0070 | g0119 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02965 | hp2 | a0009 | c0015 | t0017 | g0014 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02970 | hp1 | a0001 | c0002 | t0011 | g0050 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0087 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02976 | hp1 | a0001 | c0005 | t0042 | g0172 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0018 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03017 | hp1 | a0001 | c0001 | t0089 | g0200 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03017 | hp2 | a0001 | c0004 | t0015 | g0004 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03041 | hp2 | a0003 | c0010 | t0068 | g0053 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0024 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03130 | hp2 | a0003 | c0010 | t0018 | g0053 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03139 | hp1 | a0001 | c0002 | t0066 | g0170 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03139 | hp2 | a0007 | c0012 | t0028 | g0031 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03209 | hp2 | a0004 | c0006 | t0032 | g0101 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03225 | hp2 | a0001 | c0002 | t0011 | g0050 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03239 | hp1 | a0004 | c0006 | t0055 | g0027 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03239 | hp2 | a0002 | c0003 | t0009 | g0025 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03453 | hp1 | a0002 | c0013 | t0016 | g0182 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03486 | hp1 | a0001 | c0001 | t0026 | g0018 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03491 | hp1 | a0002 | c0003 | t0006 | g0051 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0145 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03492 | hp2 | a0002 | c0003 | t0006 | g0051 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03516 | hp1 | a0001 | c0002 | t0011 | g0169 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03516 | hp2 | a0009 | c0015 | t0017 | g0014 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03540 | hp1 | a0001 | c0005 | t0062 | g0192 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03540 | hp2 | a0004 | c0006 | t0041 | g0072 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03579 | hp1 | a0002 | c0013 | t0016 | g0042 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03654 | hp1 | a0001 | c0001 | t0015 | g0032 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03669 | hp1 | a0002 | c0003 | t0006 | g0237 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03669 | hp2 | a0002 | c0003 | t0039 | g0030 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03688 | hp1 | a0001 | c0001 | t0092 | g0001 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03688 | hp2 | a0001 | c0001 | t0021 | g0089 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03704 | hp2 | a0001 | c0001 | t0096 | g0141 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03710 | hp1 | a0001 | c0001 | t0085 | g0155 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03831 | hp1 | a0001 | c0005 | t0036 | g0109 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0144 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03834 | hp1 | a0002 | c0003 | t0006 | g0238 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03834 | hp2 | a0001 | c0001 | t0093 | g0205 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03927 | hp1 | a0024 | c0050 | t0001 | g0061 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0067 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04115 | hp1 | a0015 | c0048 | t0050 | g0244 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0003 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04204 | hp1 | a0001 | c0001 | t0022 | g0102 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04204 | hp2 | a0002 | c0003 | t0009 | g0057 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04228 | hp1 | a0002 | c0003 | t0048 | g0007 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG04228 | hp2 | a0001 | c0009 | t0009 | g0083 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18522 | hp1 | a0003 | c0010 | t0018 | g0242 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18612 | hp1 | a0001 | c0001 | t0014 | g0008 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18612 | hp2 | a0002 | c0003 | t0006 | g0236 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18747 | hp1 | a0021 | c0037 | t0002 | g0033 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18747 | hp2 | a0001 | c0001 | t0094 | g0216 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18906 | hp1 | a0007 | c0012 | t0028 | g0031 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0076 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18942 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18942 | hp2 | a0001 | c0001 | t0013 | g0115 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0068 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18945 | hp2 | a0010 | c0011 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18946 | hp1 | a0027 | c0052 | t0030 | g0211 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18946 | hp2 | a0001 | c0009 | t0010 | g0124 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18947 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18949 | hp1 | a0004 | c0006 | t0032 | g0098 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18949 | hp2 | a0014 | c0028 | t0051 | g0231 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18950 | hp1 | a0005 | c0008 | t0004 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18951 | hp1 | a0001 | c0001 | t0040 | g0176 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18952 | hp1 | a0001 | c0014 | t0029 | g0043 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18962 | hp1 | a0001 | c0014 | t0029 | g0185 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18962 | hp2 | a0005 | c0008 | t0004 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18964 | hp1 | a0001 | c0031 | t0004 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18964 | hp2 | a0023 | c0040 | t0084 | g0008 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18967 | hp1 | a0001 | c0036 | t0008 | g0135 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18967 | hp2 | a0002 | c0003 | t0071 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18970 | hp1 | a0002 | c0003 | t0010 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18970 | hp2 | a0012 | c0023 | t0025 | g0065 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18971 | hp2 | a0010 | c0011 | t0046 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18975 | hp2 | a0001 | c0014 | t0029 | g0043 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18981 | hp1 | a0002 | c0003 | t0006 | g0007 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18981 | hp2 | a0001 | c0041 | t0030 | g0210 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18982 | hp2 | a0001 | c0009 | t0065 | g0060 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18983 | hp1 | a0006 | c0007 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18983 | hp2 | a0001 | c0001 | t0063 | g0189 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18984 | hp2 | a0010 | c0011 | t0046 | g0121 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18985 | hp1 | a0002 | c0003 | t0010 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18985 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18986 | hp1 | a0005 | c0008 | t0045 | g0048 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18999 | hp2 | a0001 | c0001 | t0091 | g0059 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19000 | hp2 | a0002 | c0003 | t0010 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19002 | hp1 | a0001 | c0001 | t0043 | g0039 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19002 | hp2 | a0001 | c0001 | t0077 | g0162 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19004 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19010 | hp2 | a0001 | c0020 | t0060 | g0186 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19011 | hp1 | a0010 | c0011 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19012 | hp2 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19030 | hp1 | a0008 | c0029 | t0003 | g0075 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19030 | hp2 | a0002 | c0046 | t0001 | g0183 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19043 | hp1 | a0001 | c0001 | t0083 | g0116 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19043 | hp2 | a0001 | c0005 | t0035 | g0174 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19056 | hp1 | a0001 | c0004 | t0027 | g0196 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19057 | hp2 | a0001 | c0001 | t0030 | g0213 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19060 | hp1 | a0001 | c0001 | t0020 | g0235 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19060 | hp2 | a0012 | c0023 | t0025 | g0158 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19062 | hp2 | a0001 | c0001 | t0043 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19063 | hp2 | a0006 | c0007 | t0001 | g0191 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19064 | hp2 | a0006 | c0007 | t0001 | g0022 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19065 | hp1 | a0002 | c0003 | t0010 | g0007 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19070 | hp1 | a0001 | c0001 | t0082 | g0150 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19070 | hp2 | a0001 | c0001 | t0020 | g0228 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19079 | hp1 | a0001 | c0035 | t0079 | g0064 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19085 | hp1 | a0001 | c0009 | t0040 | g0214 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19085 | hp2 | a0006 | c0007 | t0001 | g0022 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19088 | hp2 | a0005 | c0008 | t0045 | g0048 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0090 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA19240 | hp2 | a0022 | c0039 | t0035 | g0122 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0091 | AFR | ASW | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20129 | hp2 | a0001 | c0005 | t0023 | g0112 | AFR | ASW | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20752 | hp1 | a0002 | c0047 | t0003 | g0079 | EUR | TSI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20752 | hp2 | a0003 | c0019 | t0021 | g0026 | EUR | TSI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20905 | hp1 | a0004 | c0006 | t0054 | g0096 | SAS | GIH | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0085 | SAS | GIH | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG01123 | hp2 | a0001 | c0001 | t0044 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02109 | hp1 | a0007 | c0012 | t0028 | g0129 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02109 | hp2 | a0001 | c0001 | t0081 | g0130 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18955 | hp1 | a0026 | c0027 | t0001 | g0154 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA18955 | hp2 | a0001 | c0001 | t0020 | g0230 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA20300 | hp2 | a0001 | c0001 | t0026 | g0018 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| NA21309 | hp2 | a0011 | c0018 | t0024 | g0041 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0166 | REF | REF | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| homoSapiens_grch38 | hp1 | a0001 | c0026 | t0064 | g0146 | REF | REF | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:104689739
|
G | A | 4 | a0001a0003a0004others(1): Show | 13 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
splice_region_variant | LOW | c.-10G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/23 | chr14 | 104689739 | ||||||
| chr14:104703409
|
C | T | 1 | a0027 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.622C>T | p.Pro208Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/23 | 753/7623 | 622/3750 | 208/1249 | chr14 | 104703409 | ||
| chr14:104703437
|
T | A | 1 | a0026 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.650T>A | p.Leu217Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/23 | 781/7623 | 650/3750 | 217/1249 | chr14 | 104703437 | ||
| chr14:104707316
|
C | T | 1 | a0005 | 6 | HG00609.hp2 HG01978.hp2 NA18950.hp1 others(3): Show |
missense_variant | MODERATE | c.1049C>T | p.Pro350Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1180/7623 | 1049/3750 | 350/1249 | chr14 | 104707316 | ||
| chr14:104707525
|
ACCCCAC | A | 4 | a0003a0004a0016others(1): Show | 19 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
disruptive_inframe_deletion | MODERATE | c.1280_1285delCACCCC | p.Pro427_Pro428del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1411/7623 | 1280/3750 | 427/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | |
| chr14:104707525
|
ACCCCACC others(5): Show |
A | 3 | a0002a0015a0025 | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
disruptive_inframe_deletion | MODERATE | c.1274_1285delCACCCC others(6): Show |
p.Pro425_Pro428del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1405/7623 | 1274/3750 | 425/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | |
| chr14:104707525
|
ACCCCACC others(6): Show |
A | 1 | a0014 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.1262_1274delCACCCC others(7): Show |
p.Pro421fs | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1393/7623 | 1262/3750 | 421/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | |
| chr14:104707543
|
C | T | 1 | a0025 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1276C>T | p.Pro426Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1407/7623 | 1276/3750 | 426/1249 | chr14 | 104707543 | ||
| chr14:104707547
|
CACCCCT | C | 1 | a0007 | 4 | HG02055.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1281_1286delACCCCT | p.Pro428_Leu429del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1412/7623 | 1281/3750 | 427/1249 | chr14 | 104707547 | ||
| chr14:104707615
|
G | A | 1 | a0024 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1348G>A | p.Gly450Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1479/7623 | 1348/3750 | 450/1249 | chr14 | 104707615 | ||
| chr14:104707814
|
C | T | 1 | a0011 | 3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1547C>T | p.Pro516Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1678/7623 | 1547/3750 | 516/1249 | chr14 | 104707814 | ||
| chr14:104707849
|
C | T | 1 | a0013 | 2 | HG01516.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.1582C>T | p.Pro528Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1713/7623 | 1582/3750 | 528/1249 | chr14 | 104707849 | ||
| chr14:104707859
|
C | T | 1 | a0023 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.1592C>T | p.Ala531Val | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1723/7623 | 1592/3750 | 531/1249 | chr14 | 104707859 | ||
| chr14:104709309
|
C | T | 1 | a0010 | 4 | NA18945.hp2 NA18971.hp2 NA18984.hp2 others(1): Show |
missense_variant | MODERATE | c.1978C>T | p.Arg660Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 11/23 | 2109/7623 | 1978/3750 | 660/1249 | chr14 | 104709309 | ||
| chr14:104710152
|
C | T | 1 | a0017 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2203C>T | p.Arg735Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/23 | 2334/7623 | 2203/3750 | 735/1249 | chr14 | 104710152 | ||
| chr14:104711668
|
C | T | 1 | a0022 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2458C>T | p.Arg820Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/23 | 2589/7623 | 2458/3750 | 820/1249 | chr14 | 104711668 | ||
| chr14:104712847
|
G | A | 2 | a0008a0016 | 5 | HG00642.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
missense_variant | MODERATE | c.2630G>A | p.Arg877Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2761/7623 | 2630/3750 | 877/1249 | chr14 | 104712847 | ||
| chr14:104712941
|
C | G | 1 | a0015 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2724C>G | p.Asp908Glu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2855/7623 | 2724/3750 | 908/1249 | chr14 | 104712941 | ||
| chr14:104712961
|
C | T | 1 | a0021 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2744C>T | p.Ala915Val | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2875/7623 | 2744/3750 | 915/1249 | chr14 | 104712961 | ||
| chr14:104714356
|
A | C | 1 | a0018 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.3194A>C | p.Glu1065Ala | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3325/7623 | 3194/3750 | 1065/1249 | chr14 | 104714356 | ||
| chr14:104714448
|
C | T | 2 | a0004a0012 | 9 | HG00735.hp2 HG01243.hp2 HG03209.hp2 others(6): Show |
missense_variant | MODERATE | c.3286C>T | p.Pro1096Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3417/7623 | 3286/3750 | 1096/1249 | chr14 | 104714448 | ||
| chr14:104714566
|
C | T | 1 | a0006 | 6 | HG00544.hp2 HG01943.hp1 NA18983.hp1 others(3): Show |
missense_variant | MODERATE | c.3404C>T | p.Thr1135Met | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3535/7623 | 3404/3750 | 1135/1249 | chr14 | 104714566 | ||
| chr14:104714640
|
G | A | 1 | a0009 | 4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.3478G>A | p.Gly1160Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3609/7623 | 3478/3750 | 1160/1249 | chr14 | 104714640 | ||
| chr14:104714664
|
C | CCAGGTGG others(28): Show |
1 | a0020 | 1 | HG00558.hp2 | frameshift_variant | HIGH | c.3503_3537dupCAGGTG others(29): Show |
p.Ala1180fs | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3669/7623 | 3538/3750 | 1180/1249 | INFO_REALIGN_3_PRIME | chr14 | 104714664 | |
| chr14:104714800
|
G | A | 1 | a0019 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.3638G>A | p.Arg1213Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3769/7623 | 3638/3750 | 1213/1249 | chr14 | 104714800 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:104701407
|
G | A | 2 | a0001c0014a0001c0020 | 5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
synonymous_variant | LOW | c.42G>A | p.Leu14Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 173/7623 | 42/3750 | 14/1249 | chr14 | 104701407 | ||
| chr14:104701470
|
C | T | 50 | a0001c0001a0001c0002a0001c0004others(47): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.105C>T | p.Pro35Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 236/7623 | 105/3750 | 35/1249 | chr14 | 104701470 | ||
| chr14:104701644
|
C | T | 1 | a0001c0025 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.279C>T | p.Ser93Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 410/7623 | 279/3750 | 93/1249 | chr14 | 104701644 | ||
| chr14:104707455
|
C | G | 1 | a0001c0051 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.1188C>G | p.Pro396Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1319/7623 | 1188/3750 | 396/1249 | chr14 | 104707455 | ||
| chr14:104707494
|
G | T | 2 | a0001c0004a0024c0050 | 27 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
synonymous_variant | LOW | c.1227G>T | p.Ser409Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1358/7623 | 1227/3750 | 409/1249 | chr14 | 104707494 | ||
| chr14:104707719
|
T | C | 1 | a0009c0015 | 3 | HG02280.hp2 HG02965.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1452T>C | p.Cys484Cys | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1583/7623 | 1452/3750 | 484/1249 | chr14 | 104707719 | ||
| chr14:104707773
|
A | C | 1 | a0001c0041 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.1506A>C | p.Pro502Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1637/7623 | 1506/3750 | 502/1249 | chr14 | 104707773 | ||
| chr14:104711090
|
C | T | 3 | a0001c0005a0003c0044a0022c0039 | 10 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.2322C>T | p.Thr774Thr | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/23 | 2453/7623 | 2322/3750 | 774/1249 | chr14 | 104711090 | ||
| chr14:104711649
|
C | T | 1 | a0003c0044 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.2439C>T | p.Pro813Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/23 | 2570/7623 | 2439/3750 | 813/1249 | chr14 | 104711649 | ||
| chr14:104712514
|
C | T | 2 | a0001c0038a0011c0018 | 4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.2571C>T | p.Ser857Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/23 | 2702/7623 | 2571/3750 | 857/1249 | chr14 | 104712514 | ||
| chr14:104712857
|
T | C | 46 | a0001c0001a0001c0002a0001c0004others(43): Show | 345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
synonymous_variant | LOW | c.2640T>C | p.Asp880Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2771/7623 | 2640/3750 | 880/1249 | chr14 | 104712857 | ||
| chr14:104712983
|
C | T | 1 | a0001c0036 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2766C>T | p.Arg922Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2897/7623 | 2766/3750 | 922/1249 | chr14 | 104712983 | ||
| chr14:104714228
|
T | C | 41 | a0001c0001a0001c0002a0001c0004others(38): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
synonymous_variant | LOW | c.3066T>C | p.Asp1022Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3197/7623 | 3066/3750 | 1022/1249 | chr14 | 104714228 | ||
| chr14:104714231
|
C | T | 1 | a0001c0035 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.3069C>T | p.Pro1023Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3200/7623 | 3069/3750 | 1023/1249 | chr14 | 104714231 | ||
| chr14:104714240
|
C | T | 1 | a0001c0017 | 3 | HG02615.hp1 HG02647.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.3078C>T | p.Ser1026Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3209/7623 | 3078/3750 | 1026/1249 | chr14 | 104714240 | ||
| chr14:104714270
|
T | C | 1 | a0013c0024 | 2 | HG01516.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.3108T>C | p.Leu1036Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3239/7623 | 3108/3750 | 1036/1249 | chr14 | 104714270 | ||
| chr14:104714315
|
C | T | 1 | a0001c0020 | 2 | HG02132.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.3153C>T | p.Asp1051Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3284/7623 | 3153/3750 | 1051/1249 | chr14 | 104714315 | ||
| chr14:104714369
|
A | C | 33 | a0001c0001a0001c0004a0001c0005others(30): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
synonymous_variant | LOW | c.3207A>C | p.Pro1069Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3338/7623 | 3207/3750 | 1069/1249 | chr14 | 104714369 | ||
| chr14:104714369
|
A | G | 12 | a0001c0002a0001c0022a0002c0047others(9): Show | 60 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
synonymous_variant | LOW | c.3207A>G | p.Pro1069Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3338/7623 | 3207/3750 | 1069/1249 | chr14 | 104714369 | ||
| chr14:104714846
|
G | A | 1 | a0001c0031 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.3684G>A | p.Arg1228Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3815/7623 | 3684/3750 | 1228/1249 | chr14 | 104714846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:104689664
|
G | A | 10 | a0001c0001t0020a0001c0002t0019a0001c0020t0047others(7): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/23 | 11702 | chr14 | 104689664 | |||||
| chr14:104718929
|
C | T | 1 | a0010c0011t0046 | 2 | NA18971.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*136C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3590 | chr14 | 104718929 | |||||
| chr14:104719017
|
G | A | 1 | a0001c0001t0033 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3678 | chr14 | 104719017 | |||||
| chr14:104719230
|
G | A | 8 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(5): Show | 33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3891 | chr14 | 104719230 | |||||
| chr14:104719329
|
G | T | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3990 | chr14 | 104719329 | |||||
| chr14:104719330
|
G | T | 1 | a0001c0001t0075 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3991 | chr14 | 104719330 | |||||
| chr14:104719473
|
G | T | 1 | a0001c0021t0097 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4134 | chr14 | 104719473 | |||||
| chr14:104719572
|
G | A | 1 | a0001c0001t0076 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4233 | chr14 | 104719572 | |||||
| chr14:104719685
|
ACAGGCCC others(29): Show |
A | 10 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(7): Show | 26 | HG00673.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*960delCCCCCA others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4379 | INFO_REALIGN_3_PRIME | chr14 | 104719685 | ||||
| chr14:104719773
|
C | T | 1 | a0001c0005t0042 | 2 | HG01891.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*980C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4434 | chr14 | 104719773 | |||||
| chr14:104719798
|
C | G | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0026others(4): Show | 23 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1005C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4459 | chr14 | 104719798 | |||||
| chr14:104719826
|
C | T | 14 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(11): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4487 | chr14 | 104719826 | |||||
| chr14:104719841
|
A | T | 14 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(11): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1048A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4502 | chr14 | 104719841 | |||||
| chr14:104719986
|
A | G | 29 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(26): Show | 76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1193A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4647 | chr14 | 104719986 | |||||
| chr14:104719996
|
G | A | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1203G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4657 | chr14 | 104719996 | |||||
| chr14:104720076
|
G | C | 4 | a0003c0010t0018a0003c0010t0067a0003c0010t0068others(1): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1283G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4737 | chr14 | 104720076 | |||||
| chr14:104720179
|
C | T | 1 | a0001c0001t0095 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4840 | chr14 | 104720179 | |||||
| chr14:104720329
|
T | G | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4990 | chr14 | 104720329 | |||||
| chr14:104720330
|
T | C | 1 | a0001c0001t0077 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4991 | chr14 | 104720330 | |||||
| chr14:104720336
|
A | C | 4 | a0001c0002t0011a0001c0002t0066a0009c0015t0017others(1): Show | 10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4997 | chr14 | 104720336 | |||||
| chr14:104720336
|
A | G | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1543A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4997 | chr14 | 104720336 | |||||
| chr14:104720338
|
T | G | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4999 | chr14 | 104720338 | |||||
| chr14:104720339
|
C | G | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5000 | chr14 | 104720339 | |||||
| chr14:104720342
|
C | T | 15 | a0001c0001t0003a0001c0001t0072a0001c0002t0003others(12): Show | 42 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1549C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5003 | chr14 | 104720342 | |||||
| chr14:104720343
|
G | C | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5004 | chr14 | 104720343 | |||||
| chr14:104720348
|
G | A | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1555G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5009 | chr14 | 104720348 | |||||
| chr14:104720363
|
G | A | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5024 | chr14 | 104720363 | |||||
| chr14:104720365
|
C | T | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1572C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5026 | chr14 | 104720365 | |||||
| chr14:104720371
|
C | A | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1578C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5032 | chr14 | 104720371 | |||||
| chr14:104720397
|
C | T | 1 | a0003c0010t0068 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1604C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5058 | chr14 | 104720397 | |||||
| chr14:104720398
|
G | A | 8 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(5): Show | 33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1605G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5059 | chr14 | 104720398 | |||||
| chr14:104720403
|
C | CGTCGTCC others(97): Show |
1 | a0001c0001t0038 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1636_*1637insCACG others(100): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5091 | INFO_REALIGN_3_PRIME | chr14 | 104720403 | ||||
| chr14:104720409
|
CCTCGTGT others(27): Show |
C | 2 | a0001c0022t0069a0001c0022t0070 | 2 | HG02886.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1648_*1681delAGTC others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5102 | INFO_REALIGN_3_PRIME | chr14 | 104720409 | ||||
| chr14:104720409
|
CCTCGTGT others(130): Show |
C | 2 | a0001c0001t0093a0013c0024t0037 | 2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671_*1807del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720409 | ||||
| chr14:104720430
|
G | C | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(91): Show | 285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1637G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5091 | chr14 | 104720430 | |||||
| chr14:104720435
|
C | T | 20 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(17): Show | 50 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1642C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5096 | chr14 | 104720435 | |||||
| chr14:104720439
|
G | A | 93 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(90): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1646G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5100 | chr14 | 104720439 | |||||
| chr14:104720441
|
A | C | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1648A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5102 | chr14 | 104720441 | |||||
| chr14:104720443
|
T | TCTCGTGT others(28): Show |
2 | a0001c0001t0008a0001c0036t0008 | 2 | NA18967.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720443
|
T | TCTCGTGT others(63): Show |
3 | a0001c0001t0015a0001c0001t0082a0001c0004t0015 | 6 | HG02056.hp2 HG02135.hp2 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(66): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720443
|
T | TCTCGTGT others(98): Show |
1 | a0001c0001t0091 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(101): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720443
|
T | TCTCGTGT others(28): Show |
3 | a0001c0001t0040a0001c0009t0040a0001c0009t0065 | 3 | NA18951.hp1 NA18982.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1674_*1708dupGTCT others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720443
|
TCTCGTGT others(200): Show |
T | 1 | a0013c0024t0037 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709_*1915del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720443
|
TCTCGTGT others(476): Show |
T | 1 | a0001c0001t0094 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709_*2191del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | ||||
| chr14:104720464
|
G | C | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(85): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*1671G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | chr14 | 104720464 | |||||
| chr14:104720469
|
C | T | 14 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(11): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1676C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5130 | chr14 | 104720469 | |||||
| chr14:104720473
|
G | A | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5134 | chr14 | 104720473 | |||||
| chr14:104720474
|
T | G | 5 | a0001c0001t0005a0001c0001t0026a0001c0001t0073others(2): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1681T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5135 | chr14 | 104720474 | |||||
| chr14:104720475
|
C | A | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5136 | chr14 | 104720475 | |||||
| chr14:104720478
|
CCTCGTGT others(371): Show |
C | 1 | a0001c0001t0088 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1709_*2086del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720478 | ||||
| chr14:104720499
|
G | C | 2 | a0001c0001t0072a0001c0001t0086 | 2 | HG02074.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1706G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5160 | chr14 | 104720499 | |||||
| chr14:104720499
|
GACATCTG others(95): Show |
G | 7 | a0001c0001t0027a0001c0001t0059a0001c0001t0085others(4): Show | 11 | HG00597.hp1 HG00741.hp2 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1709_*1810del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720499 | ||||
| chr14:104720502
|
A | G | 90 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(87): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*1709A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | chr14 | 104720502 | |||||
| chr14:104720509
|
T | G | 1 | a0001c0001t0072 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5170 | chr14 | 104720509 | |||||
| chr14:104720510
|
A | C | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(82): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1717A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5171 | chr14 | 104720510 | |||||
| chr14:104720512
|
T | TC | 29 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(26): Show | 61 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1720dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | ||||
| chr14:104720512
|
T | TCCTCGTG others(29): Show |
5 | a0001c0001t0008a0001c0001t0033a0001c0001t0044others(2): Show | 11 | HG00621.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1721insCTCG others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | ||||
| chr14:104720512
|
T | TCCTCGTG others(168): Show |
1 | a0005c0008t0045 | 2 | NA18986.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1720_*1721insCTCG others(171): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | ||||
| chr14:104720513
|
CTCGTGTG others(26): Show |
C | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(45): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1753delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | chr14 | 104720513 | |||||
| chr14:104720513
|
CTCGTGTG others(60): Show |
C | 4 | a0001c0005t0023a0001c0005t0062a0020c0030t0078others(1): Show | 6 | HG00558.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1787delTCGT others(63): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | chr14 | 104720513 | |||||
| chr14:104720533
|
A | G | 34 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(31): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1740A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5194 | chr14 | 104720533 | |||||
| chr14:104720544
|
A | C | 34 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(31): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1751A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5205 | chr14 | 104720544 | |||||
| chr14:104720546
|
T | TC | 33 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(30): Show | 72 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1754dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5209 | INFO_REALIGN_3_PRIME | chr14 | 104720546 | ||||
| chr14:104720547
|
CTCGTGTG others(26): Show |
C | 1 | a0001c0002t0011 | 2 | HG02809.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1755_*1787delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5209 | chr14 | 104720547 | |||||
| chr14:104720567
|
G | C | 2 | a0001c0001t0093a0013c0024t0037 | 2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1774G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5228 | chr14 | 104720567 | |||||
| chr14:104720576
|
G | A | 2 | a0001c0001t0093a0013c0024t0037 | 2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5237 | chr14 | 104720576 | |||||
| chr14:104720578
|
A | C | 81 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(78): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5239 | chr14 | 104720578 | |||||
| chr14:104720580
|
T | TC | 81 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(78): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1788dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5243 | INFO_REALIGN_3_PRIME | chr14 | 104720580 | ||||
| chr14:104720601
|
C | CACGTCTG others(98): Show |
1 | a0002c0003t0039 | 2 | HG00280.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1823_*1927dupCTCG others(101): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | ||||
| chr14:104720601
|
C | CACGTCTG others(133): Show |
13 | a0001c0001t0040a0001c0009t0009a0001c0009t0010others(10): Show | 32 | HG00323.hp1 HG00673.hp2 HG01257.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(136): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | ||||
| chr14:104720601
|
C | CACGTCTG others(238): Show |
2 | a0002c0003t0048a0002c0003t0049 | 2 | HG01106.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(241): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | ||||
| chr14:104720601
|
C | G | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(83): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5262 | chr14 | 104720601 | |||||
| chr14:104720639
|
G | A | 1 | a0001c0001t0087 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5300 | chr14 | 104720639 | |||||
| chr14:104720649
|
TC | T | 3 | a0001c0038t0024a0011c0018t0024a0011c0018t0061 | 4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1858delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5312 | INFO_REALIGN_3_PRIME | chr14 | 104720649 | ||||
| chr14:104720671
|
G | C | 1 | a0013c0024t0037 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5332 | chr14 | 104720671 | |||||
| chr14:104720683
|
G | A | 2 | a0001c0001t0075a0001c0004t0080 | 2 | HG00280.hp1 HG00544.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1890G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5344 | chr14 | 104720683 | |||||
| chr14:104720684
|
TC | T | 8 | a0001c0001t0075a0001c0004t0080a0001c0014t0029others(5): Show | 11 | HG00280.hp1 HG00544.hp1 HG02132.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1893delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5347 | INFO_REALIGN_3_PRIME | chr14 | 104720684 | ||||
| chr14:104720718
|
G | A | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(46): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1925G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5379 | chr14 | 104720718 | |||||
| chr14:104720719
|
T | TC | 23 | a0001c0001t0007a0001c0001t0012a0001c0001t0027others(20): Show | 41 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1927dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | ||||
| chr14:104720719
|
T | TCCTCGTG others(29): Show |
7 | a0001c0001t0063a0003c0043t0025a0004c0006t0032others(4): Show | 10 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | ||||
| chr14:104720719
|
T | TCCTCGTG others(99): Show |
1 | a0004c0006t0054 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(102): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | ||||
| chr14:104720719
|
T | TCCTCGTG others(99): Show |
1 | a0002c0003t0031 | 2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(102): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | ||||
| chr14:104720720
|
CTCGTGTG others(26): Show |
C | 13 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(10): Show | 40 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1928_*1960delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | chr14 | 104720720 | |||||
| chr14:104720753
|
T | TC | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(74): Show | 244 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1961dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5416 | INFO_REALIGN_3_PRIME | chr14 | 104720753 | ||||
| chr14:104720753
|
TCTCGTGT others(62): Show |
T | 1 | a0001c0002t0058 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065_*2133delTCGT others(65): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720753 | ||||
| chr14:104720785
|
C | CGTCCTCG others(362): Show |
1 | a0001c0004t0080 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1995_*1996insCTCG others(365): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5450 | INFO_REALIGN_3_PRIME | chr14 | 104720785 | ||||
| chr14:104720786
|
G | A | 4 | a0001c0001t0027a0001c0001t0095a0001c0004t0027others(1): Show | 6 | HG00597.hp1 HG02071.hp1 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1993G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5447 | chr14 | 104720786 | |||||
| chr14:104720787
|
T | TC | 10 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(7): Show | 24 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1995dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5450 | INFO_REALIGN_3_PRIME | chr14 | 104720787 | ||||
| chr14:104720787
|
TCTCGTGT others(28): Show |
T | 2 | a0001c0005t0023a0001c0022t0070 | 3 | HG02257.hp2 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2030_*2064delCTCG others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5484 | INFO_REALIGN_3_PRIME | chr14 | 104720787 | ||||
| chr14:104720801
|
T | A | 1 | a0001c0001t0075 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5462 | chr14 | 104720801 | |||||
| chr14:104720806
|
T | C | 1 | a0001c0001t0075 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2013T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5467 | chr14 | 104720806 | |||||
| chr14:104720813
|
C | A | 1 | a0001c0001t0043 | 2 | NA19002.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2020C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5474 | chr14 | 104720813 | |||||
| chr14:104720820
|
G | A | 1 | a0001c0002t0034 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2027G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5481 | chr14 | 104720820 | |||||
| chr14:104720821
|
TC | T | 27 | a0001c0001t0003a0001c0001t0005a0001c0001t0026others(24): Show | 69 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2030delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5484 | INFO_REALIGN_3_PRIME | chr14 | 104720821 | ||||
| chr14:104720822
|
CCTCGTGT others(27): Show |
C | 2 | a0001c0022t0069a0013c0024t0037 | 2 | HG01981.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2065_*2098delTCGT others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720822 | ||||
| chr14:104720846
|
G | A | 1 | a0011c0018t0061 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5507 | chr14 | 104720846 | |||||
| chr14:104720854
|
C | T | 6 | a0001c0001t0036a0001c0001t0059a0001c0005t0036others(3): Show | 7 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2061C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5515 | chr14 | 104720854 | |||||
| chr14:104720856
|
T | TC | 9 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(6): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2064dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720856 | ||||
| chr14:104720886
|
G | A | 1 | a0002c0003t0048 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5547 | chr14 | 104720886 | |||||
| chr14:104720891
|
C | CCTCGTGT others(27): Show |
1 | a0001c0001t0063 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2100_*2133dupTCGT others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5588 | INFO_REALIGN_3_PRIME | chr14 | 104720891 | ||||
| chr14:104720925
|
TC | T | 9 | a0001c0001t0085a0001c0001t0095a0003c0043t0025others(6): Show | 12 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2134delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5588 | INFO_REALIGN_3_PRIME | chr14 | 104720925 | ||||
| chr14:104720934
|
G | T | 1 | a0001c0001t0075 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5595 | chr14 | 104720934 | |||||
| chr14:104720947
|
G | C | 1 | a0001c0001t0094 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2154G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5608 | chr14 | 104720947 | |||||
| chr14:104720965
|
G | C | 6 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(3): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5626 | chr14 | 104720965 | |||||
| chr14:104721000
|
C | G | 20 | a0001c0001t0005a0001c0001t0026a0001c0001t0063others(17): Show | 40 | HG00735.hp2 HG01074.hp1 HG01243.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5661 | chr14 | 104721000 | |||||
| chr14:104721003
|
T | C | 1 | a0013c0024t0037 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2210T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5664 | chr14 | 104721003 | |||||
| chr14:104721024
|
GCGTCGTC others(2): Show |
G | 6 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(3): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2235_*2243delCGTC others(5): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5689 | INFO_REALIGN_3_PRIME | chr14 | 104721024 | ||||
| chr14:104721024
|
GCGTCGTC others(36): Show |
G | 1 | a0013c0024t0037 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235_*2277delCGTC others(39): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5689 | INFO_REALIGN_3_PRIME | chr14 | 104721024 | ||||
| chr14:104721035
|
G | C | 1 | a0001c0001t0063 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5696 | chr14 | 104721035 | |||||
| chr14:104721038
|
T | C | 1 | a0013c0024t0037 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2245T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5699 | chr14 | 104721038 | |||||
| chr14:104721059
|
GCGTAGTC others(1): Show |
G | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(85): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*2270_*2277delAGTC others(4): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5724 | INFO_REALIGN_3_PRIME | chr14 | 104721059 | ||||
| chr14:104721061
|
G | A | 1 | a0001c0001t0026 | 3 | HG02976.hp2 HG03486.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2268G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5722 | chr14 | 104721061 | |||||
| chr14:104721063
|
A | C | 10 | a0001c0001t0063a0001c0001t0085a0003c0043t0025others(7): Show | 14 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2270A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5724 | chr14 | 104721063 | |||||
| chr14:104721065
|
T | TCCTCCTG others(29): Show |
7 | a0003c0043t0025a0004c0006t0032a0004c0006t0041others(4): Show | 10 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274insCTCC others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | INFO_REALIGN_3_PRIME | chr14 | 104721065 | ||||
| chr14:104721066
|
C | CCTCGTGT others(90): Show |
1 | a0005c0008t0045 | 2 | NA18986.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274insCTCG others(93): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | chr14 | 104721066 | |||||
| chr14:104721067
|
T | G | 7 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(4): Show | 20 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2274T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | chr14 | 104721067 | |||||
| chr14:104721069
|
G | C | 1 | a0001c0001t0085 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5730 | chr14 | 104721069 | |||||
| chr14:104721089
|
G | T | 6 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(3): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2296G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5750 | chr14 | 104721089 | |||||
| chr14:104721097
|
A | C | 1 | a0001c0001t0085 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2304A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5758 | chr14 | 104721097 | |||||
| chr14:104721118
|
T | C | 6 | a0001c0001t0005a0001c0001t0026a0001c0001t0072others(3): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2325T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5779 | chr14 | 104721118 | |||||
| chr14:104721131
|
C | T | 1 | a0001c0001t0038 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2338C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5792 | chr14 | 104721131 | |||||
| chr14:104721132
|
G | A | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5793 | chr14 | 104721132 | |||||
| chr14:104721182
|
A | G | 16 | a0001c0001t0003a0001c0001t0063a0001c0002t0003others(13): Show | 44 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2389A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5843 | chr14 | 104721182 | |||||
| chr14:104721188
|
G | A | 8 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(5): Show | 33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2395G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5849 | chr14 | 104721188 | |||||
| chr14:104721230
|
C | T | 14 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(11): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2437C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5891 | chr14 | 104721230 | |||||
| chr14:104721290
|
C | T | 1 | a0001c0001t0057 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5951 | chr14 | 104721290 | |||||
| chr14:104721325
|
G | A | 118 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(115): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*2532G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5986 | chr14 | 104721325 | |||||
| chr14:104721511
|
T | G | 1 | a0001c0035t0079 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2718T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6172 | chr14 | 104721511 | |||||
| chr14:104721645
|
T | A | 2 | a0001c0005t0035a0022c0039t0035 | 2 | NA19043.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2852T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6306 | chr14 | 104721645 | |||||
| chr14:104721690
|
A | G | 1 | a0003c0010t0067 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2897A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6351 | chr14 | 104721690 | |||||
| chr14:104721712
|
C | T | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2919C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6373 | chr14 | 104721712 | |||||
| chr14:104721894
|
G | A | 3 | a0001c0001t0030a0001c0041t0030a0027c0052t0030 | 3 | NA18946.hp1 NA18981.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3101G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6555 | chr14 | 104721894 | |||||
| chr14:104721903
|
C | T | 4 | a0001c0002t0011a0001c0002t0066a0009c0015t0017others(1): Show | 10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3110C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6564 | chr14 | 104721903 | |||||
| chr14:104721997
|
A | G | 1 | a0001c0009t0065 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3204A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6658 | chr14 | 104721997 | |||||
| chr14:104722122
|
T | G | 2 | a0004c0006t0055a0004c0006t0056 | 2 | HG01243.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3329T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6783 | chr14 | 104722122 | |||||
| chr14:104722126
|
G | A | 1 | a0001c0001t0073 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3333G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6787 | chr14 | 104722126 | |||||
| chr14:104722177
|
G | A | 1 | a0001c0002t0066 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3384G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6838 | chr14 | 104722177 | |||||
| chr14:104722207
|
T | C | 1 | a0004c0006t0055 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3414T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6868 | chr14 | 104722207 | |||||
| chr14:104722244
|
C | T | 1 | a0001c0001t0089 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3451C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6905 | chr14 | 104722244 | |||||
| chr14:104722273
|
G | A | 2 | a0001c0005t0035a0022c0039t0035 | 2 | NA19043.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3480G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6934 | chr14 | 104722273 | |||||
| chr14:104722364
|
T | A | 1 | a0002c0003t0071 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3571T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 7025 | chr14 | 104722364 | |||||
| chr14:104722499
|
G | A | 14 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(11): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3706G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 7160 | chr14 | 104722499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:104689843
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0055others(23): Show | 40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10+104G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104689843 | ||||||
| chr14:104690040
|
C | A | 1 | a0004c0006t0041g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+301C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690040 | ||||||
| chr14:104690073
|
G | A | 40 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(37): Show | 54 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.-10+334G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690073 | ||||||
| chr14:104690156
|
T | C | 1 | a0001c0001t0038g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-10+417T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690156 | ||||||
| chr14:104690336
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-10+597C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690336 | ||||||
| chr14:104690419
|
A | G | 142 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0188others(139): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.-10+680A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690419 | ||||||
| chr14:104690443
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 6 | NA18973.hp1 NA18979.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+704G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690443 | ||||||
| chr14:104690606
|
G | A | 45 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(42): Show | 60 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-10+867G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690606 | ||||||
| chr14:104690705
|
C | T | 45 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(42): Show | 61 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10+966C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690705 | ||||||
| chr14:104690706
|
G | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 6 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+967G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690706 | ||||||
| chr14:104690784
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0002g0187a0001c0014t0029g0043others(2): Show | 6 | HG00609.hp1 HG03704.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1045G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690784 | ||||||
| chr14:104690862
|
G | A | 1 | a0001c0001t0063g0189 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+1123G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690862 | ||||||
| chr14:104690891
|
A | G | 30 | a0001c0001t0008g0240a0001c0001t0020g0228a0001c0001t0020g0230others(27): Show | 37 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+1152A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690891 | ||||||
| chr14:104690981
|
G | A | 49 | a0001c0001t0001g0202a0001c0001t0002g0001a0001c0001t0002g0010others(46): Show | 74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10+1242G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690981 | ||||||
| chr14:104690992
|
GGGCCCTG others(4): Show |
G | 3 | a0001c0017t0005g0181a0003c0010t0018g0054a0017c0045t0018g0054 | 3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-10+1264_-10+1274d others(13): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104690992 | |||||
| chr14:104691114
|
G | C | 1 | a0013c0024t0037g0029 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-10+1375G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691114 | ||||||
| chr14:104691142
|
G | A | 5 | a0004c0006t0041g0072a0004c0006t0041g0108a0009c0015t0017g0014others(2): Show | 8 | HG00733.hp2 HG00735.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+1403G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691142 | ||||||
| chr14:104691204
|
G | A | 5 | a0001c0001t0036g0111a0001c0001t0059g0110a0001c0005t0023g0112others(2): Show | 5 | HG00741.hp2 HG01081.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1465G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691204 | ||||||
| chr14:104691328
|
G | A | 1 | a0001c0001t0002g0023 | 2 | HG00408.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-10+1589G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691328 | ||||||
| chr14:104691439
|
T | C | 1 | a0001c0009t0009g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10+1700T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691439 | ||||||
| chr14:104691470
|
G | A | 1 | a0001c0001t0020g0228 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-10+1731G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691470 | ||||||
| chr14:104691480
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0040g0176 | 2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-10+1741C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691480 | ||||||
| chr14:104691534
|
C | G | 1 | a0015c0048t0050g0244 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10+1795C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691534 | ||||||
| chr14:104691646
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0219 | 5 | NA18986.hp2 NA19009.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1907C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691646 | ||||||
| chr14:104691707
|
C | T | 43 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(40): Show | 58 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10+1968C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691707 | ||||||
| chr14:104691726
|
CA | C | 5 | a0001c0001t0001g0188a0001c0001t0002g0187a0001c0014t0029g0043others(2): Show | 6 | HG00609.hp1 HG03704.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1988delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691726 | ||||||
| chr14:104691818
|
C | T | 4 | a0002c0013t0016g0042a0002c0013t0016g0182a0002c0013t0016g0184others(1): Show | 5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2079C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691818 | ||||||
| chr14:104691974
|
G | T | 1 | a0004c0006t0041g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+2235G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691974 | ||||||
| chr14:104692034
|
A | G | 58 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(55): Show | 75 | HG00140.hp2 HG00408.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10+2295A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692034 | ||||||
| chr14:104692056
|
G | A | 1 | a0001c0001t0013g0115 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-10+2317G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692056 | ||||||
| chr14:104692088
|
G | A | 1 | a0001c0001t0083g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+2349G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692088 | ||||||
| chr14:104692101
|
C | T | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2362C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692101 | ||||||
| chr14:104692199
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0002g0187a0001c0020t0060g0186 | 3 | HG00609.hp1 HG03704.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-10+2460C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692199 | ||||||
| chr14:104692212
|
C | G | 2 | a0002c0003t0006g0052a0002c0003t0052g0241 | 3 | HG01257.hp2 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-10+2473C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692212 | ||||||
| chr14:104692473
|
G | A | 1 | a0009c0032t0017g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-10+2734G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692473 | ||||||
| chr14:104692666
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-10+2927C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692666 | ||||||
| chr14:104692671
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+2932C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692671 | ||||||
| chr14:104692690
|
C | T | 43 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(40): Show | 58 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10+2951C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692690 | ||||||
| chr14:104692691
|
G | A | 1 | a0002c0003t0049g0229 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-10+2952G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692691 | ||||||
| chr14:104692770
|
G | A | 1 | a0001c0002t0058g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10+3031G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692770 | ||||||
| chr14:104692901
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-10+3162A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692901 | ||||||
| chr14:104692961
|
A | C | 2 | a0001c0001t0038g0028a0001c0017t0005g0181 | 3 | HG01167.hp1 HG01169.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-10+3222A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692961 | ||||||
| chr14:104693183
|
T | C | 5 | a0001c0001t0038g0028a0001c0002t0058g0117a0001c0022t0069g0118others(2): Show | 6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+3444T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693183 | ||||||
| chr14:104693201
|
C | T | 4 | a0002c0013t0016g0042a0002c0013t0016g0182a0002c0013t0016g0184others(1): Show | 5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3462C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693201 | ||||||
| chr14:104693256
|
G | C | 1 | a0001c0002t0003g0074 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-10+3517G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693256 | ||||||
| chr14:104693295
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-10+3556T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693295 | ||||||
| chr14:104693372
|
T | G | 1 | a0001c0017t0005g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10+3633T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693372 | ||||||
| chr14:104693410
|
G | A | 1 | a0008c0029t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+3671G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693410 | ||||||
| chr14:104693422
|
G | A | 10 | a0001c0001t0005g0173a0001c0001t0036g0111a0001c0001t0059g0110others(7): Show | 10 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+3683G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693422 | ||||||
| chr14:104693453
|
T | A | 10 | a0001c0001t0005g0173a0001c0001t0036g0111a0001c0001t0059g0110others(7): Show | 10 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+3714T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693453 | ||||||
| chr14:104693719
|
T | C | 1 | a0001c0001t0002g0023 | 2 | HG00408.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-10+3980T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693719 | ||||||
| chr14:104693824
|
G | A | 1 | a0001c0001t0013g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-10+4085G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693824 | ||||||
| chr14:104693875
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0002g0187a0001c0020t0060g0186 | 3 | HG00609.hp1 HG03704.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-10+4136C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693875 | ||||||
| chr14:104693895
|
G | A | 1 | a0001c0001t0020g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-10+4156G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693895 | ||||||
| chr14:104694178
|
C | T | 4 | a0001c0002t0011g0167a0001c0002t0011g0168a0001c0002t0011g0169others(1): Show | 4 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4439C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694178 | ||||||
| chr14:104694377
|
G | A | 1 | a0002c0003t0006g0051 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-10+4638G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694377 | ||||||
| chr14:104694449
|
G | A | 1 | a0010c0011t0046g0121 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-10+4710G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694449 | ||||||
| chr14:104694459
|
C | T | 1 | a0001c0001t0008g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-10+4720C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694459 | ||||||
| chr14:104694499
|
C | T | 3 | a0001c0005t0023g0164a0011c0018t0024g0041a0011c0018t0061g0165 | 4 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4760C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694499 | ||||||
| chr14:104694543
|
C | G | 1 | a0001c0004t0001g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-10+4804C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694543 | ||||||
| chr14:104694565
|
G | A | 9 | a0001c0001t0005g0173a0001c0001t0036g0111a0001c0001t0059g0110others(6): Show | 9 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+4826G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694565 | ||||||
| chr14:104694571
|
G | T | 1 | a0001c0001t0094g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+4832G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694571 | ||||||
| chr14:104694642
|
G | A | 22 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0002g0023others(19): Show | 35 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+4903G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694642 | ||||||
| chr14:104694673
|
C | T | 4 | a0002c0013t0016g0042a0002c0013t0016g0182a0002c0013t0016g0184others(1): Show | 5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+4934C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694673 | ||||||
| chr14:104694716
|
G | C | 1 | a0001c0001t0094g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+4977G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694716 | ||||||
| chr14:104694844
|
G | A | 1 | a0001c0009t0010g0124 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-10+5105G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694844 | ||||||
| chr14:104694938
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(28): Show | 45 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-10+5199G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694938 | ||||||
| chr14:104694952
|
A | G | 57 | a0001c0001t0001g0070a0001c0001t0001g0161a0001c0001t0001g0163others(54): Show | 83 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-10+5213A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694952 | ||||||
| chr14:104694988
|
G | A | 2 | a0001c0002t0003g0024a0001c0002t0003g0076 | 3 | HG02723.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-10+5249G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694988 | ||||||
| chr14:104695045
|
T | C | 4 | a0002c0013t0016g0042a0002c0013t0016g0182a0002c0013t0016g0184others(1): Show | 5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5306T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695045 | ||||||
| chr14:104695052
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10+5313T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695052 | ||||||
| chr14:104695117
|
C | A | 1 | a0001c0001t0002g0193 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-10+5378C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695117 | ||||||
| chr14:104695125
|
A | C | 1 | a0014c0028t0051g0231 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-10+5386A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695125 | ||||||
| chr14:104695125
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(70): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-10+5386A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695125 | ||||||
| chr14:104695142
|
T | C | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5403T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695142 | ||||||
| chr14:104695145
|
G | A | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5406G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695145 | ||||||
| chr14:104695153
|
C | T | 1 | a0001c0001t0072g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+5414C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695153 | ||||||
| chr14:104695198
|
G | A | 9 | a0001c0001t0005g0173a0001c0001t0036g0111a0001c0001t0059g0110others(6): Show | 9 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+5459G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695198 | ||||||
| chr14:104695238
|
C | T | 1 | a0001c0001t0004g0215 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-10+5499C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695238 | ||||||
| chr14:104695239
|
G | A | 1 | a0001c0001t0091g0059 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+5500G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695239 | ||||||
| chr14:104695299
|
C | CA | 4 | a0001c0001t0001g0188a0001c0001t0002g0187a0001c0020t0047g0239others(1): Show | 4 | HG00609.hp1 HG02132.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5561dupA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695299 | |||||
| chr14:104695311
|
C | T | 3 | a0001c0002t0058g0117a0001c0022t0069g0118a0001c0022t0070g0119 | 3 | HG00639.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10+5572C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695311 | ||||||
| chr14:104695337
|
C | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(45): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-10+5598C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695337 | ||||||
| chr14:104695377
|
C | T | 1 | a0004c0006t0032g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10+5638C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695377 | ||||||
| chr14:104695427
|
C | T | 1 | a0001c0001t0020g0228 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-10+5688C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695427 | ||||||
| chr14:104695446
|
C | T | 1 | a0018c0034t0001g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+5707C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695446 | ||||||
| chr14:104695463
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10+5724G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695463 | ||||||
| chr14:104695580
|
A | ACACCCCT others(12): Show |
4 | a0002c0003t0006g0052a0002c0003t0006g0238a0002c0003t0049g0229others(1): Show | 5 | HG00323.hp1 HG01106.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-5776_-9-5775ins others(19): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695580 | |||||
| chr14:104695580
|
A | ACACCCCT others(28): Show |
24 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(21): Show | 34 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-9-5776_-9-5775ins others(35): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695580 | |||||
| chr14:104695582
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(25): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-5775T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695582 | ||||||
| chr14:104695582
|
T | TCTCCTCC others(25): Show |
14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0126others(11): Show | 18 | HG01074.hp1 HG01255.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-5746_-9-5745ins others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695582 | |||||
| chr14:104695587
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-9-5770T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695587 | ||||||
| chr14:104695717
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(90): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9-5640T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695717 | ||||||
| chr14:104695822
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-5535G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695822 | ||||||
| chr14:104695920
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(164): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.-9-5437C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695920 | ||||||
| chr14:104695956
|
G | A | 2 | a0001c0002t0003g0077a0001c0002t0003g0123 | 2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-9-5401G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695956 | ||||||
| chr14:104696006
|
T | C | 15 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0222others(12): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-5351T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696006 | ||||||
| chr14:104696011
|
C | T | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5346C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696011 | ||||||
| chr14:104696049
|
G | A | 5 | a0001c0001t0001g0128a0003c0010t0018g0242a0007c0012t0001g0127others(2): Show | 6 | HG02055.hp1 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5308G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696049 | ||||||
| chr14:104696082
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0026g0018 | 4 | HG02976.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5275G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696082 | ||||||
| chr14:104696125
|
T | C | 173 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(170): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.-9-5232T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696125 | ||||||
| chr14:104696156
|
T | A | 20 | a0001c0001t0005g0173a0001c0001t0036g0111a0001c0001t0059g0110others(17): Show | 22 | HG00735.hp2 HG00741.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-5201T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696156 | ||||||
| chr14:104696224
|
C | T | 3 | a0001c0001t0002g0187a0001c0020t0047g0239a0001c0020t0060g0186 | 3 | HG00609.hp1 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9-5133C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696224 | ||||||
| chr14:104696470
|
C | A | 13 | a0002c0003t0006g0051a0002c0003t0006g0232a0002c0003t0006g0233others(10): Show | 15 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-4887C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696470 | ||||||
| chr14:104696544
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-9-4813C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696544 | ||||||
| chr14:104696640
|
G | A | 3 | a0001c0001t0002g0187a0001c0020t0047g0239a0001c0020t0060g0186 | 3 | HG00609.hp1 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9-4717G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696640 | ||||||
| chr14:104696735
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-9-4622G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696735 | ||||||
| chr14:104696742
|
C | G | 2 | a0002c0013t0016g0042a0002c0013t0016g0184 | 3 | HG02572.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9-4615C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696742 | ||||||
| chr14:104696805
|
A | G | 170 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(167): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-9-4552A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696805 | ||||||
| chr14:104696991
|
C | T | 1 | a0001c0009t0040g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9-4366C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696991 | ||||||
| chr14:104697027
|
G | A | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4330G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697027 | ||||||
| chr14:104697090
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(31): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-4267C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697090 | ||||||
| chr14:104697195
|
C | T | 111 | a0001c0001t0001g0202a0001c0001t0001g0221a0001c0001t0002g0001others(108): Show | 145 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.-9-4162C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697195 | ||||||
| chr14:104697209
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-9-4148G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697209 | ||||||
| chr14:104697223
|
T | C | 147 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(144): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9-4134T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697223 | ||||||
| chr14:104697279
|
G | A | 2 | a0008c0016t0002g0045a0008c0016t0002g0198 | 3 | HG00642.hp2 HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-9-4078G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697279 | ||||||
| chr14:104697501
|
T | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0137a0001c0001t0001g0140others(10): Show | 13 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-3856T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697501 | ||||||
| chr14:104697515
|
G | T | 1 | a0001c0002t0066g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-3842G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697515 | ||||||
| chr14:104697533
|
C | A | 1 | a0001c0020t0060g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-9-3824C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697533 | ||||||
| chr14:104697729
|
C | T | 2 | a0001c0001t0001g0134a0001c0036t0008g0135 | 2 | HG02027.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-9-3628C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697729 | ||||||
| chr14:104697780
|
C | T | 1 | a0007c0012t0028g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9-3577C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697780 | ||||||
| chr14:104697861
|
C | A | 2 | a0001c0001t0038g0028a0013c0024t0037g0029 | 4 | HG01167.hp1 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-3496C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697861 | ||||||
| chr14:104697888
|
G | T | 60 | a0001c0001t0001g0202a0001c0001t0002g0001a0001c0001t0002g0010others(57): Show | 84 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-3469G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697888 | ||||||
| chr14:104697894
|
G | C | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-3463G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697894 | ||||||
| chr14:104697896
|
T | G | 1 | a0001c0005t0042g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9-3461T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697896 | ||||||
| chr14:104697906
|
G | A | 1 | a0002c0003t0031g0234 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9-3451G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697906 | ||||||
| chr14:104697948
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0096g0141 | 3 | HG00323.hp2 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-9-3409G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697948 | ||||||
| chr14:104698032
|
G | C | 1 | a0001c0001t0005g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9-3325G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698032 | ||||||
| chr14:104698043
|
G | A | 1 | a0001c0002t0058g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-3314G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698043 | ||||||
| chr14:104698131
|
G | A | 1 | a0001c0005t0023g0164 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9-3226G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698131 | ||||||
| chr14:104698194
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-9-3163C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698194 | ||||||
| chr14:104698334
|
C | G | 1 | a0001c0002t0058g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-3023C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698334 | ||||||
| chr14:104698338
|
C | G | 26 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0173others(23): Show | 35 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9-3019C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698338 | ||||||
| chr14:104698380
|
G | C | 1 | a0003c0043t0025g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9-2977G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698380 | ||||||
| chr14:104698418
|
C | T | 1 | a0008c0016t0002g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-9-2939C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698418 | ||||||
| chr14:104698597
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(31): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-2760C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698597 | ||||||
| chr14:104698806
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0014g0035 | 3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-9-2551G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698806 | ||||||
| chr14:104698893
|
A | G | 53 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0005g0011others(50): Show | 63 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-9-2464A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698893 | ||||||
| chr14:104699201
|
C | T | 1 | a0001c0001t0008g0068 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-9-2156C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699201 | ||||||
| chr14:104699242
|
C | T | 4 | a0001c0001t0012g0091a0001c0001t0012g0092a0001c0001t0012g0093others(1): Show | 4 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-2115C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699242 | ||||||
| chr14:104699448
|
G | A | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1909G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699448 | ||||||
| chr14:104699480
|
G | A | 3 | a0003c0010t0018g0053a0003c0010t0018g0242a0003c0010t0068g0053 | 3 | HG03041.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-1877G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699480 | ||||||
| chr14:104699535
|
G | C | 51 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0005g0011others(48): Show | 61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1822G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699535 | ||||||
| chr14:104699665
|
A | G | 51 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0005g0011others(48): Show | 61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1692A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699665 | ||||||
| chr14:104699679
|
G | A | 1 | a0001c0004t0001g0020 | 2 | NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-9-1678G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699679 | ||||||
| chr14:104699769
|
G | A | 51 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0005g0011others(48): Show | 61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1588G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699769 | ||||||
| chr14:104699785
|
A | G | 51 | a0001c0001t0001g0134a0001c0001t0001g0221a0001c0001t0005g0011others(48): Show | 61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1572A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699785 | ||||||
| chr14:104699915
|
C | T | 61 | a0001c0001t0001g0202a0001c0001t0002g0001a0001c0001t0002g0010others(58): Show | 85 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-9-1442C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699915 | ||||||
| chr14:104699937
|
T | C | 141 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0134others(138): Show | 190 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-9-1420T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699937 | ||||||
| chr14:104700113
|
G | A | 1 | a0001c0001t0013g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-9-1244G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700113 | ||||||
| chr14:104700171
|
C | T | 2 | a0011c0018t0024g0041a0011c0018t0061g0165 | 3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9-1186C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700171 | ||||||
| chr14:104700500
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9-857C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700500 | ||||||
| chr14:104700522
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9-835C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700522 | ||||||
| chr14:104700683
|
A | T | 48 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0173others(45): Show | 58 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9-674A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700683 | ||||||
| chr14:104700775
|
C | T | 42 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0173others(39): Show | 52 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.-9-582C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700775 | ||||||
| chr14:104700785
|
G | C | 3 | a0001c0001t0005g0223a0001c0001t0005g0224a0001c0001t0005g0225 | 3 | HG01891.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-9-572G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700785 | ||||||
| chr14:104700980
|
C | T | 49 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0173others(46): Show | 59 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9-377C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700980 | ||||||
| chr14:104701117
|
G | T | 1 | a0001c0022t0070g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9-240G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701117 | ||||||
| chr14:104701118
|
C | G | 1 | a0001c0001t0030g0213 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-9-239C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701118 | ||||||
| chr14:104701320
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0163 | 2 | HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-9-37C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701320 | ||||||
| chr14:104701762
|
C | T | 12 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0222others(9): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.391+6C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701762 | ||||||
| chr14:104701773
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0004t0001g0004others(12): Show | 27 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.391+17G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701773 | ||||||
| chr14:104701774
|
A | T | 5 | a0001c0001t0012g0090a0001c0002t0011g0167a0001c0002t0011g0168others(2): Show | 5 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+18A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701774 | ||||||
| chr14:104701818
|
G | A | 1 | a0001c0001t0007g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.391+62G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701818 | ||||||
| chr14:104701879
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.391+123G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701879 | ||||||
| chr14:104702077
|
C | T | 127 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(124): Show | 172 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.391+321C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702077 | ||||||
| chr14:104702084
|
A | G | 5 | a0001c0014t0029g0043a0001c0014t0029g0185a0001c0020t0047g0239others(2): Show | 6 | HG00609.hp2 HG02132.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+328A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702084 | ||||||
| chr14:104702091
|
C | T | 38 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0222others(35): Show | 48 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.391+335C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702091 | ||||||
| chr14:104702093
|
G | A | 11 | a0001c0001t0012g0090a0001c0002t0011g0168a0001c0002t0011g0169others(8): Show | 14 | HG00733.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+337G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702093 | ||||||
| chr14:104702178
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.391+422C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702178 | ||||||
| chr14:104702201
|
G | C | 1 | a0001c0014t0029g0185 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.391+445G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702201 | ||||||
| chr14:104702234
|
C | T | 1 | a0013c0024t0037g0029 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.391+478C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702234 | ||||||
| chr14:104702258
|
C | T | 1 | a0001c0002t0011g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.391+502C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702258 | ||||||
| chr14:104702438
|
A | G | 24 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(21): Show | 39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.392-667A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702438 | ||||||
| chr14:104702502
|
T | C | 149 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(146): Show | 196 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.392-603T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702502 | ||||||
| chr14:104702556
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.392-549T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702556 | ||||||
| chr14:104702622
|
ACAGAGGC others(22): Show |
A | 1 | a0001c0001t0012g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.392-479_392-451del others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 104702622 | |||||
| chr14:104702748
|
T | C | 1 | a0001c0001t0091g0059 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.392-357T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702748 | ||||||
| chr14:104702858
|
C | G | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-247C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702858 | ||||||
| chr14:104702875
|
C | T | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-230C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702875 | ||||||
| chr14:104702914
|
G | A | 1 | a0002c0047t0003g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.392-191G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702914 | ||||||
| chr14:104702915
|
G | T | 1 | a0001c0001t0085g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.392-190G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702915 | ||||||
| chr14:104702968
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0104a0001c0001t0001g0105 | 5 | NA18973.hp1 NA18979.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-137G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702968 | ||||||
| chr14:104703666
|
T | G | 37 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(34): Show | 51 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.667+212T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703666 | ||||||
| chr14:104703769
|
C | T | 1 | a0027c0052t0030g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.668-147C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703769 | ||||||
| chr14:104703771
|
GCATGATG others(2): Show |
G | 10 | a0003c0019t0021g0026a0003c0019t0022g0095a0004c0006t0032g0098others(7): Show | 11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-144_668-136del others(9): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703771 | ||||||
| chr14:104703781
|
T | G | 10 | a0003c0019t0021g0026a0003c0019t0022g0095a0004c0006t0032g0098others(7): Show | 11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-135T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703781 | ||||||
| chr14:104703826
|
G | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(21): Show | 38 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.668-90G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703826 | ||||||
| chr14:104703838
|
T | G | 26 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(23): Show | 41 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.668-78T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703838 | ||||||
| chr14:104703870
|
C | T | 1 | a0001c0001t0038g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.668-46C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703870 | ||||||
| chr14:104703884
|
C | T | 17 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(14): Show | 18 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.668-32C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703884 | ||||||
| chr14:104703885
|
G | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(21): Show | 38 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.668-31G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703885 | ||||||
| chr14:104703976
|
C | T | 6 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+27C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104703976 | ||||||
| chr14:104704175
|
T | C | 2 | a0002c0003t0010g0012a0002c0003t0071g0012 | 4 | NA18967.hp2 NA18970.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+226T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704175 | ||||||
| chr14:104704230
|
C | G | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.701+281C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704230 | ||||||
| chr14:104704293
|
G | T | 1 | a0027c0052t0030g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+344G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704293 | ||||||
| chr14:104704294
|
T | G | 1 | a0027c0052t0030g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+345T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704294 | ||||||
| chr14:104704323
|
G | C | 1 | a0001c0004t0001g0144 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.701+374G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704323 | ||||||
| chr14:104704415
|
C | T | 1 | a0001c0001t0012g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.701+466C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704415 | ||||||
| chr14:104704426
|
C | T | 1 | a0001c0004t0001g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.701+477C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704426 | ||||||
| chr14:104704429
|
C | T | 1 | a0005c0008t0045g0048 | 2 | NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.701+480C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704429 | ||||||
| chr14:104704555
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.701+606G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704555 | ||||||
| chr14:104704617
|
A | G | 1 | a0027c0052t0030g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+668A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704617 | ||||||
| chr14:104704657
|
G | A | 1 | a0001c0001t0073g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701+708G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704657 | ||||||
| chr14:104704685
|
C | A | 11 | a0003c0019t0021g0026a0003c0019t0022g0095a0003c0043t0025g0100others(8): Show | 12 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+736C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704685 | ||||||
| chr14:104704711
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0140a0001c0001t0014g0008others(3): Show | 6 | HG02056.hp2 NA18612.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+762C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704711 | ||||||
| chr14:104704725
|
A | G | 1 | a0001c0002t0058g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.701+776A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704725 | ||||||
| chr14:104704730
|
G | A | 1 | a0001c0051t0004g0201 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.701+781G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704730 | ||||||
| chr14:104704763
|
C | T | 1 | a0001c0001t0004g0017 | 3 | HG00408.hp1 NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.701+814C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704763 | ||||||
| chr14:104704793
|
A | T | 1 | a0002c0003t0006g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.701+844A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704793 | ||||||
| chr14:104704871
|
C | T | 28 | a0001c0001t0020g0235a0001c0009t0065g0060a0002c0003t0006g0007others(25): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+922C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704871 | ||||||
| chr14:104704921
|
C | T | 22 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(19): Show | 36 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+972C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704921 | ||||||
| chr14:104705030
|
T | TC | 90 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(87): Show | 118 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.702-1003dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 104705030 | |||||
| chr14:104705145
|
G | A | 56 | a0001c0001t0020g0235a0001c0002t0011g0167a0001c0002t0011g0168others(53): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.702-890G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705145 | ||||||
| chr14:104705282
|
T | C | 17 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(14): Show | 18 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.702-753T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705282 | ||||||
| chr14:104705297
|
A | T | 1 | a0026c0027t0001g0154 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.702-738A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705297 | ||||||
| chr14:104705357
|
T | C | 89 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(86): Show | 117 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.702-678T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705357 | ||||||
| chr14:104705369
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.702-666A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705369 | ||||||
| chr14:104705372
|
G | A | 1 | a0001c0004t0027g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702-663G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705372 | ||||||
| chr14:104705416
|
CA | C | 85 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0221others(82): Show | 112 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.702-607delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 104705416 | |||||
| chr14:104705475
|
A | G | 62 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(59): Show | 85 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-560A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705475 | ||||||
| chr14:104705510
|
G | A | 72 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(69): Show | 99 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.702-525G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705510 | ||||||
| chr14:104705622
|
C | A | 1 | a0001c0022t0069g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702-413C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705622 | ||||||
| chr14:104705648
|
T | C | 10 | a0003c0019t0021g0026a0003c0019t0022g0095a0004c0006t0032g0098others(7): Show | 11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-387T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705648 | ||||||
| chr14:104705978
|
G | A | 28 | a0001c0001t0020g0235a0001c0009t0065g0060a0002c0003t0006g0007others(25): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.702-57G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705978 | ||||||
| chr14:104706018
|
T | G | 1 | a0014c0028t0051g0231 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.702-17T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104706018 | ||||||
| chr14:104706020
|
G | C | 1 | a0014c0028t0051g0231 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.702-15G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104706020 | ||||||
| chr14:104706192
|
C | T | 11 | a0001c0001t0001g0159a0003c0019t0021g0026a0003c0019t0022g0095others(8): Show | 12 | HG00735.hp2 HG01099.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+16C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706192 | ||||||
| chr14:104706209
|
C | T | 4 | a0001c0014t0029g0043a0001c0014t0029g0185a0001c0020t0047g0239others(1): Show | 5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+33C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706209 | ||||||
| chr14:104706258
|
T | G | 1 | a0010c0011t0046g0121 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.843+82T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706258 | ||||||
| chr14:104706263
|
C | T | 2 | a0001c0001t0036g0111a0001c0001t0059g0110 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.843+87C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706263 | ||||||
| chr14:104706388
|
C | T | 2 | a0003c0044t0053g0099a0009c0032t0017g0107 | 2 | HG00733.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.843+212C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706388 | ||||||
| chr14:104706415
|
G | A | 11 | a0001c0001t0038g0028a0001c0002t0011g0167a0001c0002t0011g0168others(8): Show | 16 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.843+239G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706415 | ||||||
| chr14:104706470
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.843+294C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706470 | ||||||
| chr14:104706566
|
C | T | 1 | a0003c0043t0025g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.844-344C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706566 | ||||||
| chr14:104706658
|
T | C | 2 | a0011c0018t0024g0041a0011c0018t0061g0165 | 3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.844-252T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706658 | ||||||
| chr14:104706788
|
C | T | 1 | a0001c0001t0072g0227 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.844-122C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706788 | ||||||
| chr14:104706874
|
C | T | 9 | a0001c0002t0011g0167a0001c0002t0011g0168a0001c0002t0011g0169others(6): Show | 12 | HG00733.hp2 HG01074.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-36C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706874 | ||||||
| chr14:104707115
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 10 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.985+64G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707115 | ||||||
| chr14:104707116
|
G | C | 5 | a0001c0014t0029g0043a0001c0014t0029g0185a0001c0017t0005g0049others(2): Show | 7 | HG02132.hp2 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+65G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707116 | ||||||
| chr14:104707116
|
G | T | 2 | a0001c0041t0030g0210a0027c0052t0030g0211 | 2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.985+65G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707116 | ||||||
| chr14:104707117
|
G | A | 18 | a0001c0001t0001g0105a0003c0010t0018g0053a0003c0010t0018g0054others(15): Show | 19 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.985+66G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707117 | ||||||
| chr14:104707148
|
C | T | 1 | a0004c0006t0032g0098 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.985+97C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707148 | ||||||
| chr14:104708075
|
G | A | 1 | a0002c0003t0052g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1735+73G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708075 | ||||||
| chr14:104708108
|
G | A | 16 | a0001c0001t0001g0221a0001c0001t0005g0011a0001c0001t0005g0222others(13): Show | 25 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1735+106G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708108 | ||||||
| chr14:104708146
|
G | A | 1 | a0001c0001t0022g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1735+144G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708146 | ||||||
| chr14:104708261
|
C | T | 28 | a0001c0009t0010g0124a0001c0009t0065g0060a0002c0003t0006g0007others(25): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1736-175C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708261 | ||||||
| chr14:104708385
|
G | A | 9 | a0003c0019t0021g0026a0003c0019t0022g0095a0003c0043t0025g0100others(6): Show | 10 | HG01099.hp2 HG01243.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1736-51G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708385 | ||||||
| chr14:104708388
|
A | G | 1 | a0001c0001t0012g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1736-48A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708388 | ||||||
| chr14:104708394
|
C | CG | 15 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(12): Show | 16 | HG01099.hp2 HG01243.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1736-38dupG | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 104708394 | |||||
| chr14:104708638
|
C | T | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1888-33C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 9/22 | chr14 | 104708638 | ||||||
| chr14:104708748
|
A | G | 46 | a0001c0001t0001g0179a0001c0001t0005g0011a0001c0001t0005g0222others(43): Show | 59 | HG00733.hp2 HG00735.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.1949+16A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708748 | ||||||
| chr14:104708774
|
C | T | 1 | a0001c0022t0070g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1949+42C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708774 | ||||||
| chr14:104708824
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1949+92C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708824 | ||||||
| chr14:104708873
|
A | G | 4 | a0001c0014t0029g0043a0001c0014t0029g0185a0001c0020t0047g0239others(1): Show | 5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949+141A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708873 | ||||||
| chr14:104708901
|
CT | C | 25 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(22): Show | 39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1949+170delT | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708901 | ||||||
| chr14:104708903
|
G | A | 25 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0156others(22): Show | 39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1949+171G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708903 | ||||||
| chr14:104709028
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1950-253G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709028 | ||||||
| chr14:104709050
|
C | T | 72 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0086others(69): Show | 89 | HG00408.hp2 HG00639.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.1950-231C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709050 | ||||||
| chr14:104709117
|
C | T | 1 | a0001c0004t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1950-164C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709117 | ||||||
| chr14:104709210
|
G | A | 1 | a0008c0029t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1950-71G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709210 | ||||||
| chr14:104709271
|
C | A | 1 | a0008c0029t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1950-10C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709271 | ||||||
| chr14:104709717
|
C | T | 1 | a0008c0029t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2138+12C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709717 | ||||||
| chr14:104709730
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2138+25C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709730 | ||||||
| chr14:104709807
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0209 | 2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.2138+102A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709807 | ||||||
| chr14:104709898
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2139-190G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709898 | ||||||
| chr14:104710029
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2139-59C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104710029 | ||||||
| chr14:104710244
|
C | T | 1 | a0013c0024t0037g0029 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2239+56C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710244 | ||||||
| chr14:104710255
|
C | T | 1 | a0002c0003t0006g0052 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2239+67C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710255 | ||||||
| chr14:104710345
|
T | C | 28 | a0001c0001t0004g0078a0001c0002t0003g0003a0001c0002t0003g0024others(25): Show | 41 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2239+157T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710345 | ||||||
| chr14:104710346
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2239+158G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710346 | ||||||
| chr14:104710356
|
CG | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2239+170delG | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 104710356 | |||||
| chr14:104710384
|
C | A | 1 | a0002c0003t0006g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2239+196C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710384 | ||||||
| chr14:104710417
|
ACACACAC others(27): Show |
A | 2 | a0001c0001t0001g0036a0001c0001t0001g0136 | 3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2239+245_2239+278d others(36): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 104710417 | |||||
| chr14:104710435
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2239+247C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710435 | ||||||
| chr14:104710444
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2239+256G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710444 | ||||||
| chr14:104710509
|
G | A | 1 | a0001c0001t0087g0203 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2239+321G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710509 | ||||||
| chr14:104710515
|
G | A | 1 | a0001c0001t0033g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2239+327G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710515 | ||||||
| chr14:104710578
|
A | C | 3 | a0001c0002t0003g0024a0001c0002t0003g0073a0001c0002t0003g0076 | 4 | HG02622.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2240-359A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710578 | ||||||
| chr14:104710637
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2240-300G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710637 | ||||||
| chr14:104711014
|
CA | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
splice_region_variant&intron_variant | LOW | c.2310+8delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 14/22 | chr14 | 104711014 | ||||||
| chr14:104711229
|
C | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0173a0001c0001t0005g0222others(12): Show | 20 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2418+43C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711229 | ||||||
| chr14:104711273
|
C | T | 3 | a0001c0001t0030g0213a0001c0041t0030g0210a0027c0052t0030g0211 | 3 | NA18946.hp1 NA18981.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2418+87C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711273 | ||||||
| chr14:104711316
|
T | C | 2 | a0001c0041t0030g0210a0027c0052t0030g0211 | 2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2418+130T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711316 | ||||||
| chr14:104711355
|
T | A | 1 | a0001c0001t0033g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2418+169T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711355 | ||||||
| chr14:104711720
|
C | T | 1 | a0001c0020t0060g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2489+21C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711720 | ||||||
| chr14:104711752
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.2489+53T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711752 | ||||||
| chr14:104711761
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2489+62G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711761 | ||||||
| chr14:104711813
|
C | T | 2 | a0001c0009t0040g0214a0001c0009t0065g0060 | 2 | NA18982.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2489+114C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711813 | ||||||
| chr14:104711814
|
G | A | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2489+115G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711814 | ||||||
| chr14:104711816
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2489+117C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711816 | ||||||
| chr14:104711847
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0047a0001c0001t0002g0219others(3): Show | 9 | HG00597.hp2 HG02523.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489+148C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711847 | ||||||
| chr14:104711991
|
C | T | 1 | a0013c0024t0037g0029 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2489+292C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711991 | ||||||
| chr14:104712080
|
A | G | 7 | a0003c0010t0018g0053a0003c0010t0018g0054a0003c0010t0018g0242others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2490-353A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712080 | ||||||
| chr14:104712132
|
G | A | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490-301G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712132 | ||||||
| chr14:104712141
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.2490-292T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712141 | ||||||
| chr14:104712146
|
C | T | 1 | a0002c0003t0006g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2490-287C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712146 | ||||||
| chr14:104712270
|
C | T | 1 | a0001c0004t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2490-163C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712270 | ||||||
| chr14:104712273
|
C | T | 1 | a0001c0004t0014g0062 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2490-160C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712273 | ||||||
| chr14:104712397
|
C | T | 1 | a0003c0043t0025g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2490-36C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712397 | ||||||
| chr14:104712706
|
G | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.2611-122G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712706 | ||||||
| chr14:104712744
|
G | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 261 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.2611-84G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712744 | ||||||
| chr14:104712775
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0040g0176 | 2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2611-53G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712775 | ||||||
| chr14:104712786
|
G | A | 1 | a0001c0002t0003g0081 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2611-42G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712786 | ||||||
| chr14:104712787
|
C | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 5 | HG02922.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2611-41C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712787 | ||||||
| chr14:104713007
|
C | T | 18 | a0001c0001t0005g0011a0001c0001t0005g0173a0001c0001t0005g0222others(15): Show | 25 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2775+15C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713007 | ||||||
| chr14:104713010
|
G | A | 1 | a0001c0001t0007g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2775+18G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713010 | ||||||
| chr14:104713124
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2776-83G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713124 | ||||||
| chr14:104713126
|
C | G | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2776-81C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713126 | ||||||
| chr14:104713184
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2776-23C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713184 | ||||||
| chr14:104713330
|
C | G | 1 | a0001c0005t0042g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2878+21C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713330 | ||||||
| chr14:104713331
|
G | T | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2878+22G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713331 | ||||||
| chr14:104713332
|
G | A | 1 | a0009c0032t0017g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2878+23G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713332 | ||||||
| chr14:104713370
|
C | T | 12 | a0001c0001t0036g0111a0001c0001t0059g0110a0001c0005t0023g0112others(9): Show | 12 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2878+61C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713370 | ||||||
| chr14:104713417
|
C | T | 1 | a0001c0001t0007g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2879-28C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713417 | ||||||
| chr14:104713748
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0081g0130 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3040+142G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713748 | ||||||
| chr14:104713892
|
C | A | 2 | a0009c0015t0017g0014a0009c0032t0017g0107 | 4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3040+286C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713892 | ||||||
| chr14:104713967
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0137a0001c0001t0001g0171others(4): Show | 7 | HG02056.hp2 NA18612.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.3041-236T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713967 | ||||||
| chr14:104714057
|
C | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0159a0001c0001t0001g0161others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.3041-146C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714057 | ||||||
| chr14:104714128
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0038others(11): Show | 19 | HG01255.hp2 HG01358.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.3041-75G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714128 | ||||||
| chr14:104714131
|
A | G | 3 | a0001c0002t0003g0024a0001c0002t0003g0073a0001c0002t0003g0076 | 4 | HG02622.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3041-72A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714131 | ||||||
| chr14:104714147
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.3041-56C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714147 | ||||||
| chr14:104714962
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3694+106A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104714962 | ||||||
| chr14:104714979
|
G | A | 1 | a0001c0002t0003g0024 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3694+123G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104714979 | ||||||
| chr14:104715200
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0073g0226 | 2 | HG01884.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3695-84C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104715200 | ||||||
| chr14:104715233
|
G | A | 1 | a0001c0002t0058g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3695-51G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104715233 | ||||||
| chr14:104715455
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.*1+115G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715455 | ||||||
| chr14:104715511
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.*1+171A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715511 | ||||||
| chr14:104715514
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.*1+174C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715514 | ||||||
| chr14:104715525
|
C | T | 12 | a0001c0001t0036g0111a0001c0001t0059g0110a0001c0005t0023g0112others(9): Show | 12 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.*1+185C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715525 | ||||||
| chr14:104715565
|
C | T | 2 | a0001c0001t0001g0128a0007c0012t0001g0127 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*1+225C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715565 | ||||||
| chr14:104715601
|
G | A | 1 | a0001c0001t0083g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*1+261G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715601 | ||||||
| chr14:104715642
|
C | G | 1 | a0001c0005t0062g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*1+302C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715642 | ||||||
| chr14:104715649
|
C | T | 3 | a0001c0001t0005g0173a0001c0001t0005g0222a0001c0001t0074g0131 | 3 | HG02258.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*1+309C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715649 | ||||||
| chr14:104715653
|
CCCTGGGG others(28): Show |
C | 1 | a0001c0001t0075g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*1+315_*1+349delCT others(33): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104715653 | |||||
| chr14:104715668
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.*1+328G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715668 | ||||||
| chr14:104715714
|
G | A | 2 | a0001c0002t0003g0081a0001c0002t0003g0085 | 2 | NA18994.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.*1+374G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715714 | ||||||
| chr14:104715754
|
C | T | 1 | a0015c0048t0050g0244 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*1+414C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715754 | ||||||
| chr14:104715969
|
C | A | 1 | a0013c0024t0037g0029 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.*1+629C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715969 | ||||||
| chr14:104716118
|
C | T | 1 | a0008c0029t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*1+778C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716118 | ||||||
| chr14:104716123
|
G | A | 7 | a0001c0002t0011g0050a0001c0002t0011g0167a0001c0002t0011g0168others(4): Show | 10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*1+783G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716123 | ||||||
| chr14:104716125
|
T | C | 1 | a0001c0004t0001g0020 | 2 | NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.*1+785T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716125 | ||||||
| chr14:104716227
|
C | G | 7 | a0001c0002t0011g0050a0001c0002t0011g0167a0001c0002t0011g0168others(4): Show | 10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*1+887C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716227 | ||||||
| chr14:104716253
|
C | T | 1 | a0001c0022t0070g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*1+913C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716253 | ||||||
| chr14:104716375
|
G | C | 1 | a0002c0003t0006g0052 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.*1+1035G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716375 | ||||||
| chr14:104716412
|
C | A | 5 | a0001c0001t0012g0090a0001c0001t0012g0091a0001c0001t0012g0092others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+1072C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716412 | ||||||
| chr14:104716428
|
G | A | 2 | a0001c0005t0042g0172a0001c0005t0042g0175 | 2 | HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*1+1088G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716428 | ||||||
| chr14:104716554
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0014g0035 | 3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*1+1214G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716554 | ||||||
| chr14:104716796
|
T | G | 1 | a0001c0001t0038g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.*1+1456T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716796 | ||||||
| chr14:104716899
|
T | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.*1+1559T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716899 | ||||||
| chr14:104716966
|
A | G | 3 | a0001c0038t0024g0178a0011c0018t0024g0041a0011c0018t0061g0165 | 4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1+1626A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716966 | ||||||
| chr14:104716992
|
C | T | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*1+1652C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716992 | ||||||
| chr14:104717065
|
C | T | 9 | a0001c0022t0069g0118a0001c0022t0070g0119a0003c0010t0018g0053others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+1725C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717065 | ||||||
| chr14:104717066
|
G | A | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*1+1726G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717066 | ||||||
| chr14:104717159
|
A | G | 1 | a0002c0003t0006g0236 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.*2-1636A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717159 | ||||||
| chr14:104717226
|
CCCGGGCA others(32): Show |
C | 10 | a0001c0002t0003g0082a0001c0005t0023g0112a0001c0005t0023g0113others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.*2-1536_*2-1498del others(39): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717226 | |||||
| chr14:104717257
|
CCGCCCCC others(31): Show |
C | 2 | a0001c0001t0059g0110a0001c0001t0093g0205 | 2 | HG00741.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.*2-1536_*2-1499del others(38): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717257 | |||||
| chr14:104717265
|
A | C | 2 | a0001c0001t0005g0225a0022c0039t0035g0122 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1530A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717265 | ||||||
| chr14:104717265
|
ACCGGGCA others(68): Show |
A | 2 | a0001c0001t0026g0018a0001c0002t0058g0117 | 4 | HG00639.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1492_*2-1418del others(75): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717265 | |||||
| chr14:104717276
|
T | C | 3 | a0001c0001t0005g0225a0001c0009t0009g0114a0022c0039t0035g0122 | 3 | HG02698.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1519T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717276 | ||||||
| chr14:104717292
|
C | T | 1 | a0022c0039t0035g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-1503C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717292 | ||||||
| chr14:104717292
|
CAGTCCCC others(30): Show |
C | 3 | a0001c0022t0069g0118a0001c0022t0070g0119a0013c0024t0037g0029 | 4 | HG01516.hp2 HG01981.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1497_*2-1461del others(37): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717292 | |||||
| chr14:104717295
|
T | TC | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.*2-1491dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | |||||
| chr14:104717295
|
T | TCCCCCCC others(69): Show |
2 | a0001c0001t0083g0116a0001c0009t0040g0214 | 2 | NA19043.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.*2-1493_*2-1418dup others(76): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | |||||
| chr14:104717295
|
T | TCCCCCCC others(70): Show |
1 | a0001c0009t0065g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.*2-1494_*2-1418dup others(77): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | |||||
| chr14:104717304
|
C | T | 16 | a0001c0002t0003g0003a0001c0002t0003g0024a0001c0002t0003g0073others(13): Show | 29 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.*2-1491C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717304 | ||||||
| chr14:104717313
|
C | T | 2 | a0001c0001t0001g0177a0022c0039t0035g0122 | 2 | NA19080.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1482C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717313 | ||||||
| chr14:104717314
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0090g0138 | 2 | HG00621.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.*2-1481G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717314 | ||||||
| chr14:104717329
|
T | C | 1 | a0022c0039t0035g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-1466T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717329 | ||||||
| chr14:104717335
|
G | GCCCCCCC others(28): Show |
2 | a0002c0013t0016g0042a0002c0013t0016g0184 | 3 | HG02572.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*2-1443_*2-1409dup others(35): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717335 | |||||
| chr14:104717349
|
G | A | 1 | a0005c0008t0002g0195 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.*2-1446G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717349 | ||||||
| chr14:104717351
|
T | C | 3 | a0001c0022t0069g0118a0001c0022t0070g0119a0013c0024t0037g0029 | 4 | HG01516.hp2 HG01981.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1444T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717351 | ||||||
| chr14:104717359
|
C | T | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-1436C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717359 | ||||||
| chr14:104717370
|
T | TCCCCCCC others(70): Show |
1 | a0001c0001t0040g0176 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.*2-1418_*2-1417ins others(77): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717370 | |||||
| chr14:104717371
|
C | T | 3 | a0004c0006t0054g0096a0004c0006t0055g0027a0004c0006t0056g0027 | 3 | HG01243.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*2-1424C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717371 | ||||||
| chr14:104717376
|
C | T | 1 | a0001c0001t0033g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.*2-1419C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717376 | ||||||
| chr14:104717377
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.*2-1418C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717377 | ||||||
| chr14:104717377
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0077g0162others(1): Show | 8 | HG00621.hp2 HG02056.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-1418C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717377 | ||||||
| chr14:104717401
|
T | C | 3 | a0001c0038t0024g0178a0011c0018t0024g0041a0011c0018t0061g0165 | 4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1394T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717401 | ||||||
| chr14:104717412
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.*2-1383A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717412 | ||||||
| chr14:104717573
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*2-1222C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717573 | ||||||
| chr14:104717576
|
CT | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0014g0197 | 3 | HG01109.hp1 HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.*2-1214delT | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717576 | |||||
| chr14:104717712
|
G | C | 2 | a0009c0015t0017g0014a0009c0032t0017g0107 | 4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.*2-1083G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717712 | ||||||
| chr14:104717751
|
G | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.*2-1044G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717751 | ||||||
| chr14:104717779
|
G | A | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-1016G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717779 | ||||||
| chr14:104717863
|
C | T | 1 | a0001c0001t0005g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*2-932C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717863 | ||||||
| chr14:104717874
|
TC | T | 12 | a0001c0001t0005g0011a0001c0001t0005g0173a0001c0001t0005g0222others(9): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.*2-915delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717874 | |||||
| chr14:104717880
|
C | T | 1 | a0001c0001t0075g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*2-915C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717880 | ||||||
| chr14:104717914
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0096g0141 | 2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*2-881C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717914 | ||||||
| chr14:104717932
|
T | A | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-863T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717932 | ||||||
| chr14:104717976
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.*2-819G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717976 | ||||||
| chr14:104718126
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.*2-669T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718126 | ||||||
| chr14:104718287
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0015g0032a0001c0001t0015g0151others(1): Show | 5 | HG02135.hp2 HG03654.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-508G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718287 | ||||||
| chr14:104718294
|
G | A | 2 | a0001c0020t0047g0239a0001c0020t0060g0186 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-501G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718294 | ||||||
| chr14:104718325
|
C | T | 11 | a0001c0001t0036g0111a0001c0001t0059g0110a0001c0005t0023g0113others(8): Show | 11 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.*2-470C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718325 | ||||||
| chr14:104718352
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.*2-443A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718352 | ||||||
| chr14:104718402
|
C | T | 2 | a0001c0001t0001g0202a0001c0004t0001g0144 | 2 | HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.*2-393C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718402 | ||||||
| chr14:104718471
|
T | C | 1 | a0001c0001t0085g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*2-324T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718471 | ||||||
| chr14:104718500
|
C | T | 1 | a0001c0001t0038g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.*2-295C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718500 | ||||||
| chr14:104718501
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.*2-294A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718501 | ||||||
| chr14:104718517
|
G | A | 7 | a0001c0002t0011g0050a0001c0002t0011g0167a0001c0002t0011g0168others(4): Show | 10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*2-278G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718517 | ||||||
| chr14:104718627
|
G | A | 1 | a0001c0001t0073g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*2-168G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718627 | ||||||
| chr14:104718746
|
TAC | T | 28 | a0001c0001t0003g0206a0001c0002t0003g0003a0001c0002t0003g0024others(25): Show | 41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.*2-48_*2-47delAC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718746 |